Canonical Allele Identifier: CA366264873

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567917A>T (hg19) ; chr6:g.158146885A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146885A>T , CM000668.2:g.158146885A>T	GRCh38
NC_000006.11:g.158567917A>T , CM000668.1:g.158567917A>T	GRCh37
NC_000006.10:g.158487905A>T	NCBI36
NG_032889.1:g.26396T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*218T>A	ENSP00000475855.1:n.*218T>A
ENST00000642244.1:c.294T>A	ENSP00000493554.1:p.Asp98Glu
ENST00000642903.1:c.384T>A	ENSP00000493559.1:p.Asp128Glu
ENST00000643093.1:n.434T>A
ENST00000644972.1:c.384T>A	ENSP00000496451.1:p.Asp128Glu
ENST00000645077.1:c.*218T>A	ENSP00000496113.1:n.*218T>A
ENST00000645172.1:c.*189+1980T>A	ENSP00000495367.1:n.*189+1980T>A
ENST00000646190.1:n.1615T>A
ENST00000646208.1:c.120T>A	ENSP00000493723.1:p.Asp40Glu
ENST00000646410.1:c.255T>A	ENSP00000494205.1:p.Asp85Glu
ENST00000646562.1:c.*218T>A	ENSP00000496087.1:n.*218T>A
ENST00000647468.2:c.384T>A MANE Select	ENSP00000496731.1:p.Asp128Glu
ENST00000648111.1:c.*28T>A	ENSP00000497275.1:n.*28T>A
ENST00000367101.5:c.384T>A	ENSP00000356068.1:p.Asp128Glu
ENST00000367104.7:c.384T>A	ENSP00000356071.3:p.Asp128Glu
ENST00000606965.5:c.384T>A	ENSP00000475808.1:p.Asp128Glu
ENST00000607000.1:c.384T>A	ENSP00000475788.1:p.Asp128Glu
ENST00000607071.5:c.*218T>A	ENSP00000475855.1:n.*218T>A
ENST00000607742.5:c.*218T>A	ENSP00000475523.1:n.*218T>A
NM_032861.3:c.384T>A	NP_116250.3:p.Asp128Glu
NR_073096.1:n.526T>A
XM_006715586.1:c.174T>A	XP_006715649.1:p.Asp58Glu
XM_011536196.1:c.363T>A	XP_011534498.1:p.Asp121Glu
XM_011536197.1:c.384T>A	XP_011534499.1:p.Asp128Glu
XM_011536198.1:c.174T>A	XP_011534500.1:p.Asp58Glu
XR_942606.1:n.385T>A
XM_006715586.3:c.174T>A	XP_006715649.1:p.Asp58Glu
XM_011536196.3:c.363T>A	XP_011534498.1:p.Asp121Glu
XM_011536198.3:c.174T>A	XP_011534500.1:p.Asp58Glu
XM_024446573.1:c.384T>A	XP_024302341.1:p.Asp128Glu
XR_001743697.2:n.465T>A
XR_942606.2:n.516T>A
NM_032861.4:c.384T>A MANE Select	NP_116250.3:p.Asp128Glu
NR_073096.2:n.508T>A