Canonical Allele Identifier: CA1948233299

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2587626C= , CM000673.2:g.2587626C=	GRCh38
NC_000011.9:g.2608856C= , CM000673.1:g.2608856C=	GRCh37
NC_000011.8:g.2565432C=	NCBI36
NG_008935.1:g.147636C= , LRG_287:g.147636C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.828C=	ENSP00000434560.2:p.Tyr276=
ENST00000646564.2:c.645C=	ENSP00000495806.2:p.Tyr215=
ENST00000155840.12:c.1185C= MANE Select	ENSP00000155840.2:p.Tyr395=
ENST00000335475.6:c.804C=	ENSP00000334497.5:p.Tyr268=
ENST00000646564.1:c.291C=	ENSP00000495806.1:p.Tyr97=
ENST00000155840.9:c.1185C=	ENSP00000155840.2:p.Tyr395=
ENST00000335475.5:c.804C=	ENSP00000334497.5:p.Tyr268=
NM_000218.2:c.1185C= , LRG_287t1:c.1185C=	NP_000209.2:p.Tyr395=
NM_181798.1:c.804C= , LRG_287t2:c.804C=	NP_861463.1:p.Tyr268=
NM_000218.3:c.1185C= MANE Select	NP_000209.2:p.Tyr395=