Canonical Allele Identifier: CA472038459

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2604772A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583542A>G , CM000673.2:g.2583542A>G	GRCh38
NC_000011.9:g.2604772A>G , CM000673.1:g.2604772A>G	GRCh37
NC_000011.8:g.2561348A>G	NCBI36
NG_008935.1:g.143552A>G , LRG_287:g.143552A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.768A>G	ENSP00000434560.2:p.Pro256=
ENST00000646564.2:c.585A>G	ENSP00000495806.2:p.Pro195=
ENST00000155840.12:c.1029A>G MANE Select	ENSP00000155840.2:p.Pro343=
ENST00000335475.6:c.648A>G	ENSP00000334497.5:p.Pro216=
ENST00000646564.1:c.231A>G	ENSP00000495806.1:p.Pro77=
ENST00000155840.9:c.1029A>G	ENSP00000155840.2:p.Pro343=
ENST00000335475.5:c.648A>G	ENSP00000334497.5:p.Pro216=
NM_000218.2:c.1029A>G , LRG_287t1:c.1029A>G	NP_000209.2:p.Pro343=
NM_181798.1:c.648A>G , LRG_287t2:c.648A>G	NP_861463.1:p.Pro216=
NM_000218.3:c.1029A>G MANE Select	NP_000209.2:p.Pro343=