Canonical Allele Identifier: CA571467235

Gene: SERAC1

Linked Data

• gnomAD v2: 6-158535750-A-AG
• gnomAD v3: 6-158114718-A-AG
• gnomAD v4: 6-158114718-A-AG
• MyVariant Identifiers: chr6:g.158535750_158535751insG (hg19) ; chr6:g.158114718_158114719insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114718_158114719insG , CM000668.2:g.158114718_158114719insG	GRCh38
NC_000006.11:g.158535750_158535751insG , CM000668.1:g.158535750_158535751insG	GRCh37
NC_000006.10:g.158455738_158455739insG	NCBI36
NG_032889.1:g.58562_58563insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+70_*1404+71insC	ENSP00000475855.1:n.*1404+70_*1404+71insC
ENST00000642244.1:c.1594+70_1594+71insC	ENSP00000493554.1:n.1594+70_1594+71insC
ENST00000642903.1:c.1754_1755insC	ENSP00000493559.1:p.Leu586SerfsTer14
ENST00000644972.1:c.1684+70_1684+71insC	ENSP00000496451.1:n.1684+70_1684+71insC
ENST00000645077.1:c.*1305+70_*1305+71insC	ENSP00000496113.1:n.*1305+70_*1305+71insC
ENST00000645172.1:c.*1386+70_*1386+71insC	ENSP00000495367.1:n.*1386+70_*1386+71insC
ENST00000646190.1:n.3015+70_3015+71insC
ENST00000646208.1:c.1420+70_1420+71insC	ENSP00000493723.1:n.1420+70_1420+71insC
ENST00000646410.1:c.1555+70_1555+71insC	ENSP00000494205.1:n.1555+70_1555+71insC
ENST00000646562.1:c.*1588_*1589insC	ENSP00000496087.1:n.*1588_*1589insC
ENST00000647468.2:c.1684+70_1684+71insC MANE Select	ENSP00000496731.1:n.1684+70_1684+71insC
ENST00000648111.1:c.*1372+70_*1372+71insC	ENSP00000497275.1:n.*1372+70_*1372+71insC
ENST00000367104.7:c.1684+70_1684+71insC	ENSP00000356071.3:n.1684+70_1684+71insC
ENST00000435180.5:c.479_480insC	ENSP00000391168.1:p.Leu161SerfsTer?
ENST00000606965.5:c.*315_*316insC	ENSP00000475808.1:n.*315_*316insC
ENST00000607071.5:c.*1618+70_*1618+71insC	ENSP00000475855.1:n.*1618+70_*1618+71insC
ENST00000607742.5:c.*2962+70_*2962+71insC	ENSP00000475523.1:n.*2962+70_*2962+71insC
NM_032861.3:c.1684+70_1684+71insC	NP_116250.3:n.1684+70_1684+71insC
NR_073096.1:n.1687_1688insC
XM_006715586.1:c.1474+70_1474+71insC	XP_006715649.1:n.1474+70_1474+71insC
XM_011536196.1:c.1663+70_1663+71insC	XP_011534498.1:n.1663+70_1663+71insC
XM_011536197.1:c.1570+70_1570+71insC	XP_011534499.1:n.1570+70_1570+71insC
XM_011536198.1:c.1474+70_1474+71insC	XP_011534500.1:n.1474+70_1474+71insC
XM_006715586.3:c.1474+70_1474+71insC	XP_006715649.1:n.1474+70_1474+71insC
XM_011536196.3:c.1663+70_1663+71insC	XP_011534498.1:n.1663+70_1663+71insC
XM_011536198.3:c.1474+70_1474+71insC	XP_011534500.1:n.1474+70_1474+71insC
XM_024446573.1:c.1684+70_1684+71insC	XP_024302341.1:n.1684+70_1684+71insC
XR_001743697.2:n.1715+70_1715+71insC
XR_942606.2:n.1766+70_1766+71insC
NM_032861.4:c.1684+70_1684+71insC MANE Select	NP_116250.3:n.1684+70_1684+71insC
NR_073096.2:n.1669_1670insC