Canonical Allele Identifier: CA379133066

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2604736C>A (hg19) ; chr11:g.2583506C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583506C>A , CM000673.2:g.2583506C>A	GRCh38
NC_000011.9:g.2604736C>A , CM000673.1:g.2604736C>A	GRCh37
NC_000011.8:g.2561312C>A	NCBI36
NG_008935.1:g.143516C>A , LRG_287:g.143516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.732C>A	ENSP00000434560.2:p.Cys244Ter
ENST00000646564.2:c.549C>A	ENSP00000495806.2:p.Cys183Ter
ENST00000155840.12:c.993C>A MANE Select	ENSP00000155840.2:p.Cys331Ter
ENST00000335475.6:c.612C>A	ENSP00000334497.5:p.Cys204Ter
ENST00000646564.1:c.195C>A	ENSP00000495806.1:p.Cys65Ter
ENST00000155840.9:c.993C>A	ENSP00000155840.2:p.Cys331Ter
ENST00000335475.5:c.612C>A	ENSP00000334497.5:p.Cys204Ter
NM_000218.2:c.993C>A , LRG_287t1:c.993C>A	NP_000209.2:p.Cys331Ter
NM_181798.1:c.612C>A , LRG_287t2:c.612C>A	NP_861463.1:p.Cys204Ter
NM_000218.3:c.993C>A MANE Select	NP_000209.2:p.Cys331Ter