Canonical Allele Identifier: CA2840840843

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2778063G>T , CM000673.2:g.2778063G>T	GRCh38
NC_000011.9:g.2799293G>T , CM000673.1:g.2799293G>T	GRCh37
NC_000011.8:g.2755869G>T	NCBI36
NG_008935.1:g.338073G>T , LRG_287:g.338073G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1437+26G>T	ENSP00000434560.2:n.1437+26G>T
ENST00000646564.2:c.1254+26G>T	ENSP00000495806.2:n.1254+26G>T
ENST00000155840.12:c.1794+26G>T MANE Select	ENSP00000155840.2:n.1794+26G>T
ENST00000335475.6:c.1413+26G>T	ENSP00000334497.5:n.1413+26G>T
ENST00000526095.2:c.198+26G>T	ENSP00000494939.1:n.198+26G>T
ENST00000646564.1:c.900+26G>T	ENSP00000495806.1:n.900+26G>T
ENST00000155840.9:c.1794+26G>T	ENSP00000155840.2:n.1794+26G>T
ENST00000335475.5:c.1413+26G>T	ENSP00000334497.5:n.1413+26G>T
ENST00000526095.1:n.301+26G>T
NM_000218.2:c.1794+26G>T , LRG_287t1:c.1794+26G>T	NP_000209.2:n.1794+26G>T
NM_181798.1:c.1413+26G>T , LRG_287t2:c.1413+26G>T	NP_861463.1:n.1413+26G>T
NM_000218.3:c.1794+26G>T MANE Select	NP_000209.2:n.1794+26G>T