Canonical Allele Identifier: CA379131019

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2593310C>A (hg19) ; chr11:g.2572080C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572080C>A , CM000673.2:g.2572080C>A	GRCh38
NC_000011.9:g.2593310C>A , CM000673.1:g.2593310C>A	GRCh37
NC_000011.8:g.2549886C>A	NCBI36
NG_008935.1:g.132090C>A , LRG_287:g.132090C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.490C>A	ENSP00000434560.2:p.Leu164Met
ENST00000646564.2:c.478-11355C>A	ENSP00000495806.2:n.478-11355C>A
ENST00000155840.12:c.751C>A MANE Select	ENSP00000155840.2:p.Leu251Met
ENST00000335475.6:c.370C>A	ENSP00000334497.5:p.Leu124Met
ENST00000646564.1:c.124-11355C>A	ENSP00000495806.1:n.124-11355C>A
ENST00000155840.9:c.751C>A	ENSP00000155840.2:p.Leu251Met
ENST00000335475.5:c.370C>A	ENSP00000334497.5:p.Leu124Met
ENST00000496887.6:c.490C>A	ENSP00000434560.1:p.Leu164Met
NM_000218.2:c.751C>A , LRG_287t1:c.751C>A	NP_000209.2:p.Leu251Met
NM_181798.1:c.370C>A , LRG_287t2:c.370C>A	NP_861463.1:p.Leu124Met
NM_000218.3:c.751C>A MANE Select	NP_000209.2:p.Leu251Met