Canonical Allele Identifier: CA2574728133

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2570560G>C , CM000673.2:g.2570560G>C	GRCh38
NC_000011.9:g.2591790G>C , CM000673.1:g.2591790G>C	GRCh37
NC_000011.8:g.2548366G>C	NCBI36
NG_008935.1:g.130570G>C , LRG_287:g.130570G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.217-68G>C	ENSP00000434560.2:n.217-68G>C
ENST00000646564.2:c.478-12875G>C	ENSP00000495806.2:n.478-12875G>C
ENST00000155840.12:c.478-68G>C MANE Select	ENSP00000155840.2:n.478-68G>C
ENST00000335475.6:c.97-68G>C	ENSP00000334497.5:n.97-68G>C
ENST00000646564.1:c.124-12875G>C	ENSP00000495806.1:n.124-12875G>C
ENST00000155840.9:c.478-68G>C	ENSP00000155840.2:n.478-68G>C
ENST00000335475.5:c.97-68G>C	ENSP00000334497.5:n.97-68G>C
ENST00000496887.6:c.217-68G>C	ENSP00000434560.1:n.217-68G>C
NM_000218.2:c.478-68G>C , LRG_287t1:c.478-68G>C	NP_000209.2:n.478-68G>C
NM_181798.1:c.97-68G>C , LRG_287t2:c.97-68G>C	NP_861463.1:n.97-68G>C
NM_000218.3:c.478-68G>C MANE Select	NP_000209.2:n.478-68G>C