Canonical Allele Identifier: CA366255098

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535922A>T (hg19) ; chr6:g.158114890A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114890A>T , CM000668.2:g.158114890A>T	GRCh38
NC_000006.11:g.158535922A>T , CM000668.1:g.158535922A>T	GRCh37
NC_000006.10:g.158455910A>T	NCBI36
NG_032889.1:g.58391T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.795T>A	ENSP00000391168.2:n.795T>A
ENST00000607071.6:c.*1303T>A	ENSP00000475855.1:n.*1303T>A
ENST00000642244.1:c.1493T>A	ENSP00000493554.1:p.Ile498Asn
ENST00000642903.1:c.1583T>A	ENSP00000493559.1:p.Ile528Asn
ENST00000644972.1:c.1583T>A	ENSP00000496451.1:p.Ile528Asn
ENST00000645077.1:c.*1204T>A	ENSP00000496113.1:n.*1204T>A
ENST00000645172.1:c.*1285T>A	ENSP00000495367.1:n.*1285T>A
ENST00000646190.1:n.2914T>A
ENST00000646208.1:c.1319T>A	ENSP00000493723.1:p.Ile440Asn
ENST00000646410.1:c.1454T>A	ENSP00000494205.1:p.Ile485Asn
ENST00000646562.1:c.*1417T>A	ENSP00000496087.1:n.*1417T>A
ENST00000647468.2:c.1583T>A MANE Select	ENSP00000496731.1:p.Ile528Asn
ENST00000648111.1:c.*1271T>A	ENSP00000497275.1:n.*1271T>A
ENST00000367101.5:c.*31T>A	ENSP00000356068.1:n.*31T>A
ENST00000367104.7:c.1583T>A	ENSP00000356071.3:p.Ile528Asn
ENST00000435180.5:c.308T>A	ENSP00000391168.1:p.Ile103Asn
ENST00000606965.5:c.*144T>A	ENSP00000475808.1:n.*144T>A
ENST00000607071.5:c.*1517T>A	ENSP00000475855.1:n.*1517T>A
ENST00000607742.5:c.*2861T>A	ENSP00000475523.1:n.*2861T>A
NM_032861.3:c.1583T>A	NP_116250.3:p.Ile528Asn
NR_073096.1:n.1516T>A
XM_006715586.1:c.1373T>A	XP_006715649.1:p.Ile458Asn
XM_011536196.1:c.1562T>A	XP_011534498.1:p.Ile521Asn
XM_011536197.1:c.1469T>A	XP_011534499.1:p.Ile490Asn
XM_011536198.1:c.1373T>A	XP_011534500.1:p.Ile458Asn
XM_006715586.3:c.1373T>A	XP_006715649.1:p.Ile458Asn
XM_011536196.3:c.1562T>A	XP_011534498.1:p.Ile521Asn
XM_011536198.3:c.1373T>A	XP_011534500.1:p.Ile458Asn
XM_024446573.1:c.1583T>A	XP_024302341.1:p.Ile528Asn
XR_001743697.2:n.1614T>A
XR_942606.2:n.1665T>A
NM_032861.4:c.1583T>A MANE Select	NP_116250.3:p.Ile528Asn
NR_073096.2:n.1498T>A