Canonical Allele Identifier: CA379139801

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2799262G>A (hg19) ; chr11:g.2778032G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2778032G>A , CM000673.2:g.2778032G>A	GRCh38
NC_000011.9:g.2799262G>A , CM000673.1:g.2799262G>A	GRCh37
NC_000011.8:g.2755838G>A	NCBI36
NG_008935.1:g.338042G>A , LRG_287:g.338042G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1432G>A	ENSP00000434560.2:p.Asp478Asn
ENST00000646564.2:c.1249G>A	ENSP00000495806.2:p.Asp417Asn
ENST00000155840.12:c.1789G>A MANE Select	ENSP00000155840.2:p.Asp597Asn
ENST00000335475.6:c.1408G>A	ENSP00000334497.5:p.Asp470Asn
ENST00000526095.2:c.193G>A	ENSP00000494939.1:p.Asp65Asn
ENST00000646564.1:c.895G>A	ENSP00000495806.1:p.Asp299Asn
ENST00000155840.9:c.1789G>A	ENSP00000155840.2:p.Asp597Asn
ENST00000335475.5:c.1408G>A	ENSP00000334497.5:p.Asp470Asn
ENST00000526095.1:n.296G>A
NM_000218.2:c.1789G>A , LRG_287t1:c.1789G>A	NP_000209.2:p.Asp597Asn
NM_181798.1:c.1408G>A , LRG_287t2:c.1408G>A	NP_861463.1:p.Asp470Asn
NM_000218.3:c.1789G>A MANE Select	NP_000209.2:p.Asp597Asn