Canonical Allele Identifier: CA379129868

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2570667-G-T
• MyVariant Identifiers: chr11:g.2591897G>T (hg19) ; chr11:g.2570667G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2570667G>T , CM000673.2:g.2570667G>T	GRCh38
NC_000011.9:g.2591897G>T , CM000673.1:g.2591897G>T	GRCh37
NC_000011.8:g.2548473G>T	NCBI36
NG_008935.1:g.130677G>T , LRG_287:g.130677G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.256G>T	ENSP00000434560.2:p.Val86Phe
ENST00000646564.2:c.478-12768G>T	ENSP00000495806.2:n.478-12768G>T
ENST00000155840.12:c.517G>T MANE Select	ENSP00000155840.2:p.Val173Phe
ENST00000335475.6:c.136G>T	ENSP00000334497.5:p.Val46Phe
ENST00000646564.1:c.124-12768G>T	ENSP00000495806.1:n.124-12768G>T
ENST00000155840.9:c.517G>T	ENSP00000155840.2:p.Val173Phe
ENST00000335475.5:c.136G>T	ENSP00000334497.5:p.Val46Phe
ENST00000496887.6:c.256G>T	ENSP00000434560.1:p.Val86Phe
NM_000218.2:c.517G>T , LRG_287t1:c.517G>T	NP_000209.2:p.Val173Phe
NM_181798.1:c.136G>T , LRG_287t2:c.136G>T	NP_861463.1:p.Val46Phe
NM_000218.3:c.517G>T MANE Select	NP_000209.2:p.Val173Phe