Canonical Allele Identifier: CA379134891

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588712G>C , CM000673.2:g.2588712G>C	GRCh38
NC_000011.9:g.2609942G>C , CM000673.1:g.2609942G>C	GRCh37
NC_000011.8:g.2566518G>C	NCBI36
NG_008935.1:g.148722G>C , LRG_287:g.148722G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000218.3:c.1252-1G>C MANE Select	NP_000209.2:n.1252-1G>C
ENST00000155840.12:c.1252-1G>C MANE Select	ENSP00000155840.2:n.1252-1G>C
NM_000218.2:c.1252-1G>C , LRG_287t1:c.1252-1G>C	NP_000209.2:n.1252-1G>C
NM_181798.1:c.871-1G>C , LRG_287t2:c.871-1G>C	NP_861463.1:n.871-1G>C
ENST00000155840.9:c.1252-1G>C	ENSP00000155840.2:n.1252-1G>C
ENST00000335475.5:c.871-1G>C	ENSP00000334497.5:n.871-1G>C
ENST00000335475.6:c.871-1G>C	ENSP00000334497.5:n.871-1G>C
ENST00000496887.7:c.895-1G>C	ENSP00000434560.2:n.895-1G>C
ENST00000646564.1:c.358-1G>C	ENSP00000495806.1:n.358-1G>C
ENST00000646564.2:c.712-1G>C	ENSP00000495806.2:n.712-1G>C