Canonical Allele Identifier: CA934476677

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1846549521
• gnomAD v3: 11-2769202-A-C
• gnomAD v4: 11-2769202-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2769202A>C , CM000673.2:g.2769202A>C	GRCh38
NC_000011.9:g.2790432A>C , CM000673.1:g.2790432A>C	GRCh37
NC_000011.8:g.2747008A>C	NCBI36
NG_008935.1:g.329212A>C , LRG_287:g.329212A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1233+283A>C	ENSP00000434560.2:n.1233+283A>C
ENST00000646564.2:c.1050+283A>C	ENSP00000495806.2:n.1050+283A>C
ENST00000155840.12:c.1590+283A>C MANE Select	ENSP00000155840.2:n.1590+283A>C
ENST00000335475.6:c.1209+283A>C	ENSP00000334497.5:n.1209+283A>C
ENST00000646564.1:c.696+283A>C	ENSP00000495806.1:n.696+283A>C
ENST00000155840.9:c.1590+283A>C	ENSP00000155840.2:n.1590+283A>C
ENST00000335475.5:c.1209+283A>C	ENSP00000334497.5:n.1209+283A>C
NM_000218.2:c.1590+283A>C , LRG_287t1:c.1590+283A>C	NP_000209.2:n.1590+283A>C
NM_181798.1:c.1209+283A>C , LRG_287t2:c.1209+283A>C	NP_861463.1:n.1209+283A>C
NM_000218.3:c.1590+283A>C MANE Select	NP_000209.2:n.1590+283A>C