Canonical Allele Identifier: CA674982842

Gene: KCNQ1

Linked Data

• dbSNP Id: rs543442792
• gnomAD v3: 11-2583199-G-T
• gnomAD v4: 11-2583199-G-T
• MyVariant Identifiers: chr11:g.2604429G>T (hg19) ; chr11:g.2583199G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583199G>T , CM000673.2:g.2583199G>T	GRCh38
NC_000011.9:g.2604429G>T , CM000673.1:g.2604429G>T	GRCh37
NC_000011.8:g.2561005G>T	NCBI36
NG_008935.1:g.143209G>T , LRG_287:g.143209G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.661-236G>T	ENSP00000434560.2:n.661-236G>T
ENST00000646564.2:c.478-236G>T	ENSP00000495806.2:n.478-236G>T
ENST00000155840.12:c.922-236G>T MANE Select	ENSP00000155840.2:n.922-236G>T
ENST00000335475.6:c.541-236G>T	ENSP00000334497.5:n.541-236G>T
ENST00000646564.1:c.124-236G>T	ENSP00000495806.1:n.124-236G>T
ENST00000155840.9:c.922-236G>T	ENSP00000155840.2:n.922-236G>T
ENST00000335475.5:c.541-236G>T	ENSP00000334497.5:n.541-236G>T
NM_000218.2:c.922-236G>T , LRG_287t1:c.922-236G>T	NP_000209.2:n.922-236G>T
NM_181798.1:c.541-236G>T , LRG_287t2:c.541-236G>T	NP_861463.1:n.541-236G>T
NM_000218.3:c.922-236G>T MANE Select	NP_000209.2:n.922-236G>T