Canonical Allele Identifier: CA2839553792

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2778058G>T , CM000673.2:g.2778058G>T	GRCh38
NC_000011.9:g.2799288G>T , CM000673.1:g.2799288G>T	GRCh37
NC_000011.8:g.2755864G>T	NCBI36
NG_008935.1:g.338068G>T , LRG_287:g.338068G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1437+21G>T	ENSP00000434560.2:n.1437+21G>T
ENST00000646564.2:c.1254+21G>T	ENSP00000495806.2:n.1254+21G>T
ENST00000155840.12:c.1794+21G>T MANE Select	ENSP00000155840.2:n.1794+21G>T
ENST00000335475.6:c.1413+21G>T	ENSP00000334497.5:n.1413+21G>T
ENST00000526095.2:c.198+21G>T	ENSP00000494939.1:n.198+21G>T
ENST00000646564.1:c.900+21G>T	ENSP00000495806.1:n.900+21G>T
ENST00000155840.9:c.1794+21G>T	ENSP00000155840.2:n.1794+21G>T
ENST00000335475.5:c.1413+21G>T	ENSP00000334497.5:n.1413+21G>T
ENST00000526095.1:n.301+21G>T
NM_000218.2:c.1794+21G>T , LRG_287t1:c.1794+21G>T	NP_000209.2:n.1794+21G>T
NM_181798.1:c.1413+21G>T , LRG_287t2:c.1413+21G>T	NP_861463.1:n.1413+21G>T
NM_000218.3:c.1794+21G>T MANE Select	NP_000209.2:n.1794+21G>T