Canonical Allele Identifier: CA2835790996

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2571738G>A , CM000673.2:g.2571738G>A	GRCh38
NC_000011.9:g.2592968G>A , CM000673.1:g.2592968G>A	GRCh37
NC_000011.8:g.2549544G>A	NCBI36
NG_008935.1:g.131748G>A , LRG_287:g.131748G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.423-275G>A	ENSP00000434560.2:n.423-275G>A
ENST00000646564.2:c.478-11697G>A	ENSP00000495806.2:n.478-11697G>A
ENST00000155840.12:c.684-275G>A MANE Select	ENSP00000155840.2:n.684-275G>A
ENST00000335475.6:c.303-275G>A	ENSP00000334497.5:n.303-275G>A
ENST00000646564.1:c.124-11697G>A	ENSP00000495806.1:n.124-11697G>A
ENST00000155840.9:c.684-275G>A	ENSP00000155840.2:n.684-275G>A
ENST00000335475.5:c.303-275G>A	ENSP00000334497.5:n.303-275G>A
ENST00000496887.6:c.423-275G>A	ENSP00000434560.1:n.423-275G>A
NM_000218.2:c.684-275G>A , LRG_287t1:c.684-275G>A	NP_000209.2:n.684-275G>A
NM_181798.1:c.303-275G>A , LRG_287t2:c.303-275G>A	NP_861463.1:n.303-275G>A
NM_000218.3:c.684-275G>A MANE Select	NP_000209.2:n.684-275G>A