Canonical Allele Identifier: CA379139158

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1431896118
• gnomAD v2: 11-2797238-C-T
• gnomAD v4: 11-2776008-C-T
• MyVariant Identifiers: chr11:g.2797238C>T (hg19) ; chr11:g.2776008C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2776008C>T , CM000673.2:g.2776008C>T	GRCh38
NC_000011.9:g.2797238C>T , CM000673.1:g.2797238C>T	GRCh37
NC_000011.8:g.2753814C>T	NCBI36
NG_008935.1:g.336018C>T , LRG_287:g.336018C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1282C>T	ENSP00000434560.2:p.Gln428Ter
ENST00000646564.2:c.1099C>T	ENSP00000495806.2:p.Gln367Ter
ENST00000155840.12:c.1639C>T MANE Select	ENSP00000155840.2:p.Gln547Ter
ENST00000335475.6:c.1258C>T	ENSP00000334497.5:p.Gln420Ter
ENST00000646564.1:c.745C>T	ENSP00000495806.1:p.Gln249Ter
ENST00000155840.9:c.1639C>T	ENSP00000155840.2:p.Gln547Ter
ENST00000335475.5:c.1258C>T	ENSP00000334497.5:p.Gln420Ter
NM_000218.2:c.1639C>T , LRG_287t1:c.1639C>T	NP_000209.2:p.Gln547Ter
NM_181798.1:c.1258C>T , LRG_287t2:c.1258C>T	NP_861463.1:p.Gln420Ter
NM_000218.3:c.1639C>T MANE Select	NP_000209.2:p.Gln547Ter