Canonical Allele Identifier: CA571467205

Gene: SERAC1

Linked Data

• dbSNP Id: rs1286910569
• gnomAD v2: 6-158535731-G-GATAATACATTCAAGGAATATAAAATGAT
• gnomAD v4: 6-158114699-G-GATAATACATTCAAGGAATATAAAATGAT
• MyVariant Identifiers: chr6:g.158535731_158535732insATAATACATTCAAGGAATATAAAATGAT (hg19) ; chr6:g.158114699_158114700insATAATACATTCAAGGAATATAAAATGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114716_158114717insTATAAAATGATATAATACATTCAAGGAA , CM000668.2:g.158114716_158114717insTATAAAATGATATAATACATTCAAGGAA	GRCh38
NC_000006.11:g.158535748_158535749insTATAAAATGATATAATACATTCAAGGAA , CM000668.1:g.158535748_158535749insTATAAAATGATATAATACATTCAAGGAA	GRCh37
NC_000006.10:g.158455736_158455737insTATAAAATGATATAATACATTCAAGGAA	NCBI36
NG_032889.1:g.58581_58582insATCATTTTATATTCCTTGAATGTATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+89_*1404+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000475855.1:n.*1404+89_*1404+90insATCATTTTATATTCCTTGAAT...
ENST00000642244.1:c.1594+89_1594+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000493554.1:n.1594+89_1594+90insATCATTTTATATTCCTTGAATGT...
ENST00000642903.1:c.*9_*10insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000493559.1:n.*9_*10insATCATTTTATATTCCTTGAATGTATTAT
ENST00000644972.1:c.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000496451.1:n.1684+89_1684+90insATCATTTTATATTCCTTGAATGT...
ENST00000645077.1:c.*1305+89_*1305+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000496113.1:n.*1305+89_*1305+90insATCATTTTATATTCCTTGAAT...
ENST00000645172.1:c.*1386+89_*1386+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000495367.1:n.*1386+89_*1386+90insATCATTTTATATTCCTTGAAT...
ENST00000646190.1:n.3015+89_3015+90insATCATTTTATATTCCTTGAATGTATTAT
ENST00000646208.1:c.1420+89_1420+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000493723.1:n.1420+89_1420+90insATCATTTTATATTCCTTGAATGT...
ENST00000646410.1:c.1555+89_1555+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000494205.1:n.1555+89_1555+90insATCATTTTATATTCCTTGAATGT...
ENST00000646562.1:c.*1607_*1608insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000496087.1:n.*1607_*1608insATCATTTTATATTCCTTGAATGTATTA...
ENST00000647468.2:c.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATTAT MANE Select	ENSP00000496731.1:n.1684+89_1684+90insATCATTTTATATTCCTTGAATGT...
ENST00000648111.1:c.*1372+89_*1372+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000497275.1:n.*1372+89_*1372+90insATCATTTTATATTCCTTGAAT...
ENST00000367104.7:c.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000356071.3:n.1684+89_1684+90insATCATTTTATATTCCTTGAATGT...
ENST00000435180.5:c.498_499insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000391168.1:n.498_499insATCATTTTATATTCCTTGAATGTATTAT
ENST00000606965.5:c.*334_*335insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000475808.1:n.*334_*335insATCATTTTATATTCCTTGAATGTATTAT
ENST00000607071.5:c.*1618+89_*1618+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000475855.1:n.*1618+89_*1618+90insATCATTTTATATTCCTTGAAT...
ENST00000607742.5:c.*2962+89_*2962+90insATCATTTTATATTCCTTGAATGTATTAT	ENSP00000475523.1:n.*2962+89_*2962+90insATCATTTTATATTCCTTGAAT...
NM_032861.3:c.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATTAT	NP_116250.3:n.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATTAT
NR_073096.1:n.1706_1707insATCATTTTATATTCCTTGAATGTATTAT
XM_006715586.1:c.1474+89_1474+90insATCATTTTATATTCCTTGAATGTATTAT	XP_006715649.1:n.1474+89_1474+90insATCATTTTATATTCCTTGAATGTATT...
XM_011536196.1:c.1663+89_1663+90insATCATTTTATATTCCTTGAATGTATTAT	XP_011534498.1:n.1663+89_1663+90insATCATTTTATATTCCTTGAATGTATT...
XM_011536197.1:c.1570+89_1570+90insATCATTTTATATTCCTTGAATGTATTAT	XP_011534499.1:n.1570+89_1570+90insATCATTTTATATTCCTTGAATGTATT...
XM_011536198.1:c.1474+89_1474+90insATCATTTTATATTCCTTGAATGTATTAT	XP_011534500.1:n.1474+89_1474+90insATCATTTTATATTCCTTGAATGTATT...
XM_006715586.3:c.1474+89_1474+90insATCATTTTATATTCCTTGAATGTATTAT	XP_006715649.1:n.1474+89_1474+90insATCATTTTATATTCCTTGAATGTATT...
XM_011536196.3:c.1663+89_1663+90insATCATTTTATATTCCTTGAATGTATTAT	XP_011534498.1:n.1663+89_1663+90insATCATTTTATATTCCTTGAATGTATT...
XM_011536198.3:c.1474+89_1474+90insATCATTTTATATTCCTTGAATGTATTAT	XP_011534500.1:n.1474+89_1474+90insATCATTTTATATTCCTTGAATGTATT...
XM_024446573.1:c.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATTAT	XP_024302341.1:n.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATT...
XR_001743697.2:n.1715+89_1715+90insATCATTTTATATTCCTTGAATGTATTAT
XR_942606.2:n.1766+89_1766+90insATCATTTTATATTCCTTGAATGTATTAT
NM_032861.4:c.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATTAT MANE Select	NP_116250.3:n.1684+89_1684+90insATCATTTTATATTCCTTGAATGTATTAT
NR_073096.2:n.1688_1689insATCATTTTATATTCCTTGAATGTATTAT