Canonical Allele Identifier: CA1948336830

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2823102G= , CM000673.2:g.2823102G=	GRCh38
NC_000011.9:g.2844332G= , CM000673.1:g.2844332G=	GRCh37
NC_000011.8:g.2800908G=	NCBI36
NG_008935.1:g.383112G= , LRG_287:g.383112G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1438-24665G=	ENSP00000434560.2:n.1438-24665G=
ENST00000646564.2:c.1255-16614G=	ENSP00000495806.2:n.1255-16614G=
ENST00000155840.12:c.1795-24665G= MANE Select	ENSP00000155840.2:n.1795-24665G=
ENST00000335475.6:c.1414-24665G=	ENSP00000334497.5:n.1414-24665G=
ENST00000526095.2:c.199-24665G=	ENSP00000494939.1:n.199-24665G=
ENST00000646564.1:c.901-16614G=	ENSP00000495806.1:n.901-16614G=
ENST00000155840.9:c.1795-24665G=	ENSP00000155840.2:n.1795-24665G=
ENST00000335475.5:c.1414-24665G=	ENSP00000334497.5:n.1414-24665G=
ENST00000526095.1:n.302-24665G=
NM_000218.2:c.1795-24665G= , LRG_287t1:c.1795-24665G=	NP_000209.2:n.1795-24665G=
NM_181798.1:c.1414-24665G= , LRG_287t2:c.1414-24665G=	NP_861463.1:n.1414-24665G=
NM_000218.3:c.1795-24665G= MANE Select	NP_000209.2:n.1795-24665G=