Canonical Allele Identifier: CA2612003222

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2571264-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2571264T>C , CM000673.2:g.2571264T>C	GRCh38
NC_000011.9:g.2592494T>C , CM000673.1:g.2592494T>C	GRCh37
NC_000011.8:g.2549070T>C	NCBI36
NG_008935.1:g.131274T>C , LRG_287:g.131274T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.344-61T>C	ENSP00000434560.2:n.344-61T>C
ENST00000646564.2:c.478-12171T>C	ENSP00000495806.2:n.478-12171T>C
ENST00000155840.12:c.605-61T>C MANE Select	ENSP00000155840.2:n.605-61T>C
ENST00000335475.6:c.224-61T>C	ENSP00000334497.5:n.224-61T>C
ENST00000646564.1:c.124-12171T>C	ENSP00000495806.1:n.124-12171T>C
ENST00000155840.9:c.605-61T>C	ENSP00000155840.2:n.605-61T>C
ENST00000335475.5:c.224-61T>C	ENSP00000334497.5:n.224-61T>C
ENST00000496887.6:c.344-61T>C	ENSP00000434560.1:n.344-61T>C
NM_000218.2:c.605-61T>C , LRG_287t1:c.605-61T>C	NP_000209.2:n.605-61T>C
NM_181798.1:c.224-61T>C , LRG_287t2:c.224-61T>C	NP_861463.1:n.224-61T>C
NM_000218.3:c.605-61T>C MANE Select	NP_000209.2:n.605-61T>C