Canonical Allele Identifier: CA597432463

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1486813897
• gnomAD v2: 11-2610131-C-T
• gnomAD v4: 11-2588901-C-T
• MyVariant Identifiers: chr11:g.2610131C>T (hg19) ; chr11:g.2588901C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588901C>T , CM000673.2:g.2588901C>T	GRCh38
NC_000011.9:g.2610131C>T , CM000673.1:g.2610131C>T	GRCh37
NC_000011.8:g.2566707C>T	NCBI36
NG_008935.1:g.148911C>T , LRG_287:g.148911C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1036+47C>T	ENSP00000434560.2:n.1036+47C>T
ENST00000646564.2:c.853+47C>T	ENSP00000495806.2:n.853+47C>T
ENST00000155840.12:c.1393+47C>T MANE Select	ENSP00000155840.2:n.1393+47C>T
ENST00000335475.6:c.1012+47C>T	ENSP00000334497.5:n.1012+47C>T
ENST00000646564.1:c.499+47C>T	ENSP00000495806.1:n.499+47C>T
ENST00000155840.9:c.1393+47C>T	ENSP00000155840.2:n.1393+47C>T
ENST00000335475.5:c.1012+47C>T	ENSP00000334497.5:n.1012+47C>T
NM_000218.2:c.1393+47C>T , LRG_287t1:c.1393+47C>T	NP_000209.2:n.1393+47C>T
NM_181798.1:c.1012+47C>T , LRG_287t2:c.1012+47C>T	NP_861463.1:n.1012+47C>T
NM_000218.3:c.1393+47C>T MANE Select	NP_000209.2:n.1393+47C>T