Canonical Allele Identifier: CA379135067

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2610021A>T (hg19) ; chr11:g.2588791A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588791A>T , CM000673.2:g.2588791A>T	GRCh38
NC_000011.9:g.2610021A>T , CM000673.1:g.2610021A>T	GRCh37
NC_000011.8:g.2566597A>T	NCBI36
NG_008935.1:g.148801A>T , LRG_287:g.148801A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.973A>T	ENSP00000434560.2:p.Thr325Ser
ENST00000646564.2:c.790A>T	ENSP00000495806.2:p.Thr264Ser
ENST00000155840.12:c.1330A>T MANE Select	ENSP00000155840.2:p.Thr444Ser
ENST00000335475.6:c.949A>T	ENSP00000334497.5:p.Thr317Ser
ENST00000646564.1:c.436A>T	ENSP00000495806.1:p.Thr146Ser
ENST00000155840.9:c.1330A>T	ENSP00000155840.2:p.Thr444Ser
ENST00000335475.5:c.949A>T	ENSP00000334497.5:p.Thr317Ser
NM_000218.2:c.1330A>T , LRG_287t1:c.1330A>T	NP_000209.2:p.Thr444Ser
NM_181798.1:c.949A>T , LRG_287t2:c.949A>T	NP_861463.1:p.Thr317Ser
NM_000218.3:c.1330A>T MANE Select	NP_000209.2:p.Thr444Ser