Canonical Allele Identifier: CA2680956608

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114702-A-AATACATTCAAGGAATATAAAATGAGATC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114716_158114717insTATAAAATGAGATCATACATTCAAGGAA , CM000668.2:g.158114716_158114717insTATAAAATGAGATCATACATTCAAGGAA	GRCh38
NC_000006.11:g.158535748_158535749insTATAAAATGAGATCATACATTCAAGGAA , CM000668.1:g.158535748_158535749insTATAAAATGAGATCATACATTCAAGGAA	GRCh37
NC_000006.10:g.158455736_158455737insTATAAAATGAGATCATACATTCAAGGAA	NCBI36
NG_032889.1:g.58578_58579insGATCTCATTTTATATTCCTTGAATGTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+86_*1404+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000475855.1:n.*1404+86_*1404+87insGATCTCATTTTATATTCCTTG...
ENST00000642244.1:c.1594+86_1594+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000493554.1:n.1594+86_1594+87insGATCTCATTTTATATTCCTTGAA...
ENST00000642903.1:c.*6_*7insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000493559.1:n.*6_*7insGATCTCATTTTATATTCCTTGAATGTAT
ENST00000644972.1:c.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000496451.1:n.1684+86_1684+87insGATCTCATTTTATATTCCTTGAA...
ENST00000645077.1:c.*1305+86_*1305+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000496113.1:n.*1305+86_*1305+87insGATCTCATTTTATATTCCTTG...
ENST00000645172.1:c.*1386+86_*1386+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000495367.1:n.*1386+86_*1386+87insGATCTCATTTTATATTCCTTG...
ENST00000646190.1:n.3015+86_3015+87insGATCTCATTTTATATTCCTTGAATGTAT
ENST00000646208.1:c.1420+86_1420+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000493723.1:n.1420+86_1420+87insGATCTCATTTTATATTCCTTGAA...
ENST00000646410.1:c.1555+86_1555+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000494205.1:n.1555+86_1555+87insGATCTCATTTTATATTCCTTGAA...
ENST00000646562.1:c.*1604_*1605insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000496087.1:n.*1604_*1605insGATCTCATTTTATATTCCTTGAATGTA...
ENST00000647468.2:c.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGTAT MANE Select	ENSP00000496731.1:n.1684+86_1684+87insGATCTCATTTTATATTCCTTGAA...
ENST00000648111.1:c.*1372+86_*1372+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000497275.1:n.*1372+86_*1372+87insGATCTCATTTTATATTCCTTG...
ENST00000367104.7:c.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000356071.3:n.1684+86_1684+87insGATCTCATTTTATATTCCTTGAA...
ENST00000435180.5:c.495_496insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000391168.1:n.495_496insGATCTCATTTTATATTCCTTGAATGTAT
ENST00000606965.5:c.*331_*332insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000475808.1:n.*331_*332insGATCTCATTTTATATTCCTTGAATGTAT
ENST00000607071.5:c.*1618+86_*1618+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000475855.1:n.*1618+86_*1618+87insGATCTCATTTTATATTCCTTG...
ENST00000607742.5:c.*2962+86_*2962+87insGATCTCATTTTATATTCCTTGAATGTAT	ENSP00000475523.1:n.*2962+86_*2962+87insGATCTCATTTTATATTCCTTG...
NM_032861.3:c.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGTAT	NP_116250.3:n.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGTAT
NR_073096.1:n.1703_1704insGATCTCATTTTATATTCCTTGAATGTAT
XM_006715586.1:c.1474+86_1474+87insGATCTCATTTTATATTCCTTGAATGTAT	XP_006715649.1:n.1474+86_1474+87insGATCTCATTTTATATTCCTTGAATGT...
XM_011536196.1:c.1663+86_1663+87insGATCTCATTTTATATTCCTTGAATGTAT	XP_011534498.1:n.1663+86_1663+87insGATCTCATTTTATATTCCTTGAATGT...
XM_011536197.1:c.1570+86_1570+87insGATCTCATTTTATATTCCTTGAATGTAT	XP_011534499.1:n.1570+86_1570+87insGATCTCATTTTATATTCCTTGAATGT...
XM_011536198.1:c.1474+86_1474+87insGATCTCATTTTATATTCCTTGAATGTAT	XP_011534500.1:n.1474+86_1474+87insGATCTCATTTTATATTCCTTGAATGT...
XM_006715586.3:c.1474+86_1474+87insGATCTCATTTTATATTCCTTGAATGTAT	XP_006715649.1:n.1474+86_1474+87insGATCTCATTTTATATTCCTTGAATGT...
XM_011536196.3:c.1663+86_1663+87insGATCTCATTTTATATTCCTTGAATGTAT	XP_011534498.1:n.1663+86_1663+87insGATCTCATTTTATATTCCTTGAATGT...
XM_011536198.3:c.1474+86_1474+87insGATCTCATTTTATATTCCTTGAATGTAT	XP_011534500.1:n.1474+86_1474+87insGATCTCATTTTATATTCCTTGAATGT...
XM_024446573.1:c.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGTAT	XP_024302341.1:n.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGT...
XR_001743697.2:n.1715+86_1715+87insGATCTCATTTTATATTCCTTGAATGTAT
XR_942606.2:n.1766+86_1766+87insGATCTCATTTTATATTCCTTGAATGTAT
NM_032861.4:c.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGTAT MANE Select	NP_116250.3:n.1684+86_1684+87insGATCTCATTTTATATTCCTTGAATGTAT
NR_073096.2:n.1685_1686insGATCTCATTTTATATTCCTTGAATGTAT