Canonical Allele Identifier: CA674975333

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1208391616
• gnomAD v3: 11-2573067-G-C
• gnomAD v4: 11-2573067-G-C
• MyVariant Identifiers: chr11:g.2594297G>C (hg19) ; chr11:g.2573067G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2573067G>C , CM000673.2:g.2573067G>C	GRCh38
NC_000011.9:g.2594297G>C , CM000673.1:g.2594297G>C	GRCh37
NC_000011.8:g.2550873G>C	NCBI36
NG_008935.1:g.133077G>C , LRG_287:g.133077G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.660+81G>C	ENSP00000434560.2:n.660+81G>C
ENST00000646564.2:c.478-10368G>C	ENSP00000495806.2:n.478-10368G>C
ENST00000155840.12:c.921+81G>C MANE Select	ENSP00000155840.2:n.921+81G>C
ENST00000335475.6:c.540+81G>C	ENSP00000334497.5:n.540+81G>C
ENST00000646564.1:c.124-10368G>C	ENSP00000495806.1:n.124-10368G>C
ENST00000155840.9:c.921+81G>C	ENSP00000155840.2:n.921+81G>C
ENST00000335475.5:c.540+81G>C	ENSP00000334497.5:n.540+81G>C
NM_000218.2:c.921+81G>C , LRG_287t1:c.921+81G>C	NP_000209.2:n.921+81G>C
NM_181798.1:c.540+81G>C , LRG_287t2:c.540+81G>C	NP_861463.1:n.540+81G>C
NM_000218.3:c.921+81G>C MANE Select	NP_000209.2:n.921+81G>C