Canonical Allele Identifier: CA1948349602

Gene: KCNQ1 KCNQ1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2847802C= , CM000673.2:g.2847802C=	GRCh38
NC_000011.9:g.2869032C= , CM000673.1:g.2869032C=	GRCh37
NC_000011.8:g.2825608C=	NCBI36
NG_008935.1:g.407812C= , LRG_287:g.407812C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1473C= (KCNQ1)	ENSP00000434560.2:p.Thr491=
ENST00000155840.12:c.1830C= (KCNQ1) MANE Select	ENSP00000155840.2:p.Thr610=
ENST00000335475.6:c.1449C= (KCNQ1)	ENSP00000334497.5:p.Thr483=
ENST00000526095.2:c.234C= (KCNQ1)	ENSP00000494939.1:p.Thr78=
ENST00000155840.9:c.1830C= (KCNQ1)	ENSP00000155840.2:p.Thr610=
ENST00000335475.5:c.1449C= (KCNQ1)	ENSP00000334497.5:p.Thr483=
ENST00000526095.1:n.337C= (KCNQ1)
NM_000218.2:c.1830C= , LRG_287t1:c.1830C= (KCNQ1)	NP_000209.2:p.Thr610=
NM_181798.1:c.1449C= , LRG_287t2:c.1449C= (KCNQ1)	NP_861463.1:p.Thr483=
NR_130721.1:n.778-7360G= (KCNQ1-AS1)
NM_000218.3:c.1830C= (KCNQ1) MANE Select	NP_000209.2:p.Thr610=