Canonical Allele Identifier: CA2612010802

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2777838-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2777838T>A , CM000673.2:g.2777838T>A	GRCh38
NC_000011.9:g.2799068T>A , CM000673.1:g.2799068T>A	GRCh37
NC_000011.8:g.2755644T>A	NCBI36
NG_008935.1:g.337848T>A , LRG_287:g.337848T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1376-138T>A	ENSP00000434560.2:n.1376-138T>A
ENST00000646564.2:c.1193-138T>A	ENSP00000495806.2:n.1193-138T>A
ENST00000155840.12:c.1733-138T>A MANE Select	ENSP00000155840.2:n.1733-138T>A
ENST00000335475.6:c.1352-138T>A	ENSP00000334497.5:n.1352-138T>A
ENST00000526095.2:c.136+25T>A	ENSP00000494939.1:n.136+25T>A
ENST00000646564.1:c.839-138T>A	ENSP00000495806.1:n.839-138T>A
ENST00000155840.9:c.1733-138T>A	ENSP00000155840.2:n.1733-138T>A
ENST00000335475.5:c.1352-138T>A	ENSP00000334497.5:n.1352-138T>A
ENST00000526095.1:n.239+25T>A
NM_000218.2:c.1733-138T>A , LRG_287t1:c.1733-138T>A	NP_000209.2:n.1733-138T>A
NM_181798.1:c.1352-138T>A , LRG_287t2:c.1352-138T>A	NP_861463.1:n.1352-138T>A
NM_000218.3:c.1733-138T>A MANE Select	NP_000209.2:n.1733-138T>A