Canonical Allele Identifier: CA1948236868

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2589069T= , CM000673.2:g.2589069T=	GRCh38
NC_000011.9:g.2610299T= , CM000673.1:g.2610299T=	GRCh37
NC_000011.8:g.2566875T=	NCBI36
NG_008935.1:g.149079T= , LRG_287:g.149079T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1036+215T=	ENSP00000434560.2:n.1036+215T=
ENST00000646564.2:c.853+215T=	ENSP00000495806.2:n.853+215T=
ENST00000155840.12:c.1393+215T= MANE Select	ENSP00000155840.2:n.1393+215T=
ENST00000335475.6:c.1012+215T=	ENSP00000334497.5:n.1012+215T=
ENST00000646564.1:c.499+215T=	ENSP00000495806.1:n.499+215T=
ENST00000155840.9:c.1393+215T=	ENSP00000155840.2:n.1393+215T=
ENST00000335475.5:c.1012+215T=	ENSP00000334497.5:n.1012+215T=
NM_000218.2:c.1393+215T= , LRG_287t1:c.1393+215T=	NP_000209.2:n.1393+215T=
NM_181798.1:c.1012+215T= , LRG_287t2:c.1012+215T=	NP_861463.1:n.1012+215T=
NM_000218.3:c.1393+215T= MANE Select	NP_000209.2:n.1393+215T=