Canonical Allele Identifier: CA366255099

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535923T>A (hg19) ; chr6:g.158114891T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114891T>A , CM000668.2:g.158114891T>A	GRCh38
NC_000006.11:g.158535923T>A , CM000668.1:g.158535923T>A	GRCh37
NC_000006.10:g.158455911T>A	NCBI36
NG_032889.1:g.58390A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.794A>T	ENSP00000391168.2:n.794A>T
ENST00000607071.6:c.*1302A>T	ENSP00000475855.1:n.*1302A>T
ENST00000642244.1:c.1492A>T	ENSP00000493554.1:p.Ile498Phe
ENST00000642903.1:c.1582A>T	ENSP00000493559.1:p.Ile528Phe
ENST00000644972.1:c.1582A>T	ENSP00000496451.1:p.Ile528Phe
ENST00000645077.1:c.*1203A>T	ENSP00000496113.1:n.*1203A>T
ENST00000645172.1:c.*1284A>T	ENSP00000495367.1:n.*1284A>T
ENST00000646190.1:n.2913A>T
ENST00000646208.1:c.1318A>T	ENSP00000493723.1:p.Ile440Phe
ENST00000646410.1:c.1453A>T	ENSP00000494205.1:p.Ile485Phe
ENST00000646562.1:c.*1416A>T	ENSP00000496087.1:n.*1416A>T
ENST00000647468.2:c.1582A>T MANE Select	ENSP00000496731.1:p.Ile528Phe
ENST00000648111.1:c.*1270A>T	ENSP00000497275.1:n.*1270A>T
ENST00000367101.5:c.*30A>T	ENSP00000356068.1:n.*30A>T
ENST00000367104.7:c.1582A>T	ENSP00000356071.3:p.Ile528Phe
ENST00000435180.5:c.307A>T	ENSP00000391168.1:p.Ile103Phe
ENST00000606965.5:c.*143A>T	ENSP00000475808.1:n.*143A>T
ENST00000607071.5:c.*1516A>T	ENSP00000475855.1:n.*1516A>T
ENST00000607742.5:c.*2860A>T	ENSP00000475523.1:n.*2860A>T
NM_032861.3:c.1582A>T	NP_116250.3:p.Ile528Phe
NR_073096.1:n.1515A>T
XM_006715586.1:c.1372A>T	XP_006715649.1:p.Ile458Phe
XM_011536196.1:c.1561A>T	XP_011534498.1:p.Ile521Phe
XM_011536197.1:c.1468A>T	XP_011534499.1:p.Ile490Phe
XM_011536198.1:c.1372A>T	XP_011534500.1:p.Ile458Phe
XM_006715586.3:c.1372A>T	XP_006715649.1:p.Ile458Phe
XM_011536196.3:c.1561A>T	XP_011534498.1:p.Ile521Phe
XM_011536198.3:c.1372A>T	XP_011534500.1:p.Ile458Phe
XM_024446573.1:c.1582A>T	XP_024302341.1:p.Ile528Phe
XR_001743697.2:n.1613A>T
XR_942606.2:n.1664A>T
NM_032861.4:c.1582A>T MANE Select	NP_116250.3:p.Ile528Phe
NR_073096.2:n.1497A>T