Canonical Allele Identifier: CA2680956380

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114677-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114677T>A , CM000668.2:g.158114677T>A	GRCh38
NC_000006.11:g.158535709T>A , CM000668.1:g.158535709T>A	GRCh37
NC_000006.10:g.158455697T>A	NCBI36
NG_032889.1:g.58604A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+112A>T	ENSP00000475855.1:n.*1404+112A>T
ENST00000642244.1:c.1594+112A>T	ENSP00000493554.1:n.1594+112A>T
ENST00000642903.1:c.*32A>T	ENSP00000493559.1:n.*32A>T
ENST00000644972.1:c.1684+112A>T	ENSP00000496451.1:n.1684+112A>T
ENST00000645077.1:c.*1305+112A>T	ENSP00000496113.1:n.*1305+112A>T
ENST00000645172.1:c.*1386+112A>T	ENSP00000495367.1:n.*1386+112A>T
ENST00000646190.1:n.3015+112A>T
ENST00000646208.1:c.1420+112A>T	ENSP00000493723.1:n.1420+112A>T
ENST00000646410.1:c.1555+112A>T	ENSP00000494205.1:n.1555+112A>T
ENST00000646562.1:c.*1630A>T	ENSP00000496087.1:n.*1630A>T
ENST00000647468.2:c.1684+112A>T MANE Select	ENSP00000496731.1:n.1684+112A>T
ENST00000648111.1:c.*1372+112A>T	ENSP00000497275.1:n.*1372+112A>T
ENST00000367104.7:c.1684+112A>T	ENSP00000356071.3:n.1684+112A>T
ENST00000606965.5:c.*357A>T	ENSP00000475808.1:n.*357A>T
ENST00000607071.5:c.*1618+112A>T	ENSP00000475855.1:n.*1618+112A>T
ENST00000607742.5:c.*2962+112A>T	ENSP00000475523.1:n.*2962+112A>T
NM_032861.3:c.1684+112A>T	NP_116250.3:n.1684+112A>T
NR_073096.1:n.1729A>T
XM_006715586.1:c.1474+112A>T	XP_006715649.1:n.1474+112A>T
XM_011536196.1:c.1663+112A>T	XP_011534498.1:n.1663+112A>T
XM_011536197.1:c.1570+112A>T	XP_011534499.1:n.1570+112A>T
XM_011536198.1:c.1474+112A>T	XP_011534500.1:n.1474+112A>T
XM_006715586.3:c.1474+112A>T	XP_006715649.1:n.1474+112A>T
XM_011536196.3:c.1663+112A>T	XP_011534498.1:n.1663+112A>T
XM_011536198.3:c.1474+112A>T	XP_011534500.1:n.1474+112A>T
XM_024446573.1:c.1684+112A>T	XP_024302341.1:n.1684+112A>T
XR_001743697.2:n.1715+112A>T
XR_942606.2:n.1766+112A>T
NM_032861.4:c.1684+112A>T MANE Select	NP_116250.3:n.1684+112A>T
NR_073096.2:n.1711A>T