Canonical Allele Identifier: CA2574728254

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2587489-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2587489G>T , CM000673.2:g.2587489G>T	GRCh38
NC_000011.9:g.2608719G>T , CM000673.1:g.2608719G>T	GRCh37
NC_000011.8:g.2565295G>T	NCBI36
NG_008935.1:g.147499G>T , LRG_287:g.147499G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.772-81G>T	ENSP00000434560.2:n.772-81G>T
ENST00000646564.2:c.589-81G>T	ENSP00000495806.2:n.589-81G>T
ENST00000155840.12:c.1129-81G>T MANE Select	ENSP00000155840.2:n.1129-81G>T
ENST00000335475.6:c.748-81G>T	ENSP00000334497.5:n.748-81G>T
ENST00000646564.1:c.235-81G>T	ENSP00000495806.1:n.235-81G>T
ENST00000155840.9:c.1129-81G>T	ENSP00000155840.2:n.1129-81G>T
ENST00000335475.5:c.748-81G>T	ENSP00000334497.5:n.748-81G>T
NM_000218.2:c.1129-81G>T , LRG_287t1:c.1129-81G>T	NP_000209.2:n.1129-81G>T
NM_181798.1:c.748-81G>T , LRG_287t2:c.748-81G>T	NP_861463.1:n.748-81G>T
NM_000218.3:c.1129-81G>T MANE Select	NP_000209.2:n.1129-81G>T