Canonical Allele Identifier: CA2612008801

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2769015-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2769015G>C , CM000673.2:g.2769015G>C	GRCh38
NC_000011.9:g.2790245G>C , CM000673.1:g.2790245G>C	GRCh37
NC_000011.8:g.2746821G>C	NCBI36
NG_008935.1:g.329025G>C , LRG_287:g.329025G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1233+96G>C	ENSP00000434560.2:n.1233+96G>C
ENST00000646564.2:c.1050+96G>C	ENSP00000495806.2:n.1050+96G>C
ENST00000155840.12:c.1590+96G>C MANE Select	ENSP00000155840.2:n.1590+96G>C
ENST00000335475.6:c.1209+96G>C	ENSP00000334497.5:n.1209+96G>C
ENST00000646564.1:c.696+96G>C	ENSP00000495806.1:n.696+96G>C
ENST00000155840.9:c.1590+96G>C	ENSP00000155840.2:n.1590+96G>C
ENST00000335475.5:c.1209+96G>C	ENSP00000334497.5:n.1209+96G>C
NM_000218.2:c.1590+96G>C , LRG_287t1:c.1590+96G>C	NP_000209.2:n.1590+96G>C
NM_181798.1:c.1209+96G>C , LRG_287t2:c.1209+96G>C	NP_861463.1:n.1209+96G>C
NM_000218.3:c.1590+96G>C MANE Select	NP_000209.2:n.1590+96G>C