Canonical Allele Identifier: CA379135128

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2610057T>A (hg19) ; chr11:g.2588827T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588827T>A , CM000673.2:g.2588827T>A	GRCh38
NC_000011.9:g.2610057T>A , CM000673.1:g.2610057T>A	GRCh37
NC_000011.8:g.2566633T>A	NCBI36
NG_008935.1:g.148837T>A , LRG_287:g.148837T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1009T>A	ENSP00000434560.2:p.Phe337Ile
ENST00000646564.2:c.826T>A	ENSP00000495806.2:p.Phe276Ile
ENST00000155840.12:c.1366T>A MANE Select	ENSP00000155840.2:p.Phe456Ile
ENST00000335475.6:c.985T>A	ENSP00000334497.5:p.Phe329Ile
ENST00000646564.1:c.472T>A	ENSP00000495806.1:p.Phe158Ile
ENST00000155840.9:c.1366T>A	ENSP00000155840.2:p.Phe456Ile
ENST00000335475.5:c.985T>A	ENSP00000334497.5:p.Phe329Ile
NM_000218.2:c.1366T>A , LRG_287t1:c.1366T>A	NP_000209.2:p.Phe456Ile
NM_181798.1:c.985T>A , LRG_287t2:c.985T>A	NP_861463.1:p.Phe329Ile
NM_000218.3:c.1366T>A MANE Select	NP_000209.2:p.Phe456Ile