Canonical Allele Identifier: CA2840840846

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2778106T>A , CM000673.2:g.2778106T>A	GRCh38
NC_000011.9:g.2799336T>A , CM000673.1:g.2799336T>A	GRCh37
NC_000011.8:g.2755912T>A	NCBI36
NG_008935.1:g.338116T>A , LRG_287:g.338116T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1437+69T>A	ENSP00000434560.2:n.1437+69T>A
ENST00000646564.2:c.1254+69T>A	ENSP00000495806.2:n.1254+69T>A
ENST00000155840.12:c.1794+69T>A MANE Select	ENSP00000155840.2:n.1794+69T>A
ENST00000335475.6:c.1413+69T>A	ENSP00000334497.5:n.1413+69T>A
ENST00000526095.2:c.198+69T>A	ENSP00000494939.1:n.198+69T>A
ENST00000646564.1:c.900+69T>A	ENSP00000495806.1:n.900+69T>A
ENST00000155840.9:c.1794+69T>A	ENSP00000155840.2:n.1794+69T>A
ENST00000335475.5:c.1413+69T>A	ENSP00000334497.5:n.1413+69T>A
ENST00000526095.1:n.301+69T>A
NM_000218.2:c.1794+69T>A , LRG_287t1:c.1794+69T>A	NP_000209.2:n.1794+69T>A
NM_181798.1:c.1413+69T>A , LRG_287t2:c.1413+69T>A	NP_861463.1:n.1413+69T>A
NM_000218.3:c.1794+69T>A MANE Select	NP_000209.2:n.1794+69T>A