Canonical Allele Identifier: CA1948160962

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2445339C= , CM000673.2:g.2445339C=	GRCh38
NC_000011.9:g.2466569C= , CM000673.1:g.2466569C=	GRCh37
NC_000011.8:g.2423145C=	NCBI36
NG_008935.1:g.5349C= , LRG_287:g.5349C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.24-44C=	ENSP00000434560.2:n.24-44C=
ENST00000646564.2:c.241C=	ENSP00000495806.2:p.Pro81=
ENST00000155840.12:c.241C= MANE Select	ENSP00000155840.2:p.Pro81=
ENST00000155840.9:c.241C=	ENSP00000155840.2:p.Pro81=
ENST00000345015.4:n.18C=
ENST00000496887.6:c.24-44C=	ENSP00000434560.1:n.24-44C=
NM_000218.2:c.241C= , LRG_287t1:c.241C=	NP_000209.2:p.Pro81=
NM_000218.3:c.241C= MANE Select	NP_000209.2:p.Pro81=