Canonical Allele Identifier: CA366255037

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535895G>T (hg19) ; chr6:g.158114863G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114863G>T , CM000668.2:g.158114863G>T	GRCh38
NC_000006.11:g.158535895G>T , CM000668.1:g.158535895G>T	GRCh37
NC_000006.10:g.158455883G>T	NCBI36
NG_032889.1:g.58418C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.822C>A	ENSP00000391168.2:n.822C>A
ENST00000607071.6:c.*1330C>A	ENSP00000475855.1:n.*1330C>A
ENST00000642244.1:c.1520C>A	ENSP00000493554.1:p.Ser507Ter
ENST00000642903.1:c.1610C>A	ENSP00000493559.1:p.Ser537Ter
ENST00000644972.1:c.1610C>A	ENSP00000496451.1:p.Ser537Ter
ENST00000645077.1:c.*1231C>A	ENSP00000496113.1:n.*1231C>A
ENST00000645172.1:c.*1312C>A	ENSP00000495367.1:n.*1312C>A
ENST00000646190.1:n.2941C>A
ENST00000646208.1:c.1346C>A	ENSP00000493723.1:p.Ser449Ter
ENST00000646410.1:c.1481C>A	ENSP00000494205.1:p.Ser494Ter
ENST00000646562.1:c.*1444C>A	ENSP00000496087.1:n.*1444C>A
ENST00000647468.2:c.1610C>A MANE Select	ENSP00000496731.1:p.Ser537Ter
ENST00000648111.1:c.*1298C>A	ENSP00000497275.1:n.*1298C>A
ENST00000367101.5:c.*58C>A	ENSP00000356068.1:n.*58C>A
ENST00000367104.7:c.1610C>A	ENSP00000356071.3:p.Ser537Ter
ENST00000435180.5:c.335C>A	ENSP00000391168.1:p.Ser112Ter
ENST00000606965.5:c.*171C>A	ENSP00000475808.1:n.*171C>A
ENST00000607071.5:c.*1544C>A	ENSP00000475855.1:n.*1544C>A
ENST00000607742.5:c.*2888C>A	ENSP00000475523.1:n.*2888C>A
NM_032861.3:c.1610C>A	NP_116250.3:p.Ser537Ter
NR_073096.1:n.1543C>A
XM_006715586.1:c.1400C>A	XP_006715649.1:p.Ser467Ter
XM_011536196.1:c.1589C>A	XP_011534498.1:p.Ser530Ter
XM_011536197.1:c.1496C>A	XP_011534499.1:p.Ser499Ter
XM_011536198.1:c.1400C>A	XP_011534500.1:p.Ser467Ter
XM_006715586.3:c.1400C>A	XP_006715649.1:p.Ser467Ter
XM_011536196.3:c.1589C>A	XP_011534498.1:p.Ser530Ter
XM_011536198.3:c.1400C>A	XP_011534500.1:p.Ser467Ter
XM_024446573.1:c.1610C>A	XP_024302341.1:p.Ser537Ter
XR_001743697.2:n.1641C>A
XR_942606.2:n.1692C>A
NM_032861.4:c.1610C>A MANE Select	NP_116250.3:p.Ser537Ter
NR_073096.2:n.1525C>A