Canonical Allele Identifier: CA379133896

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2606514C>A (hg19) ; chr11:g.2585284C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2585284C>A , CM000673.2:g.2585284C>A	GRCh38
NC_000011.9:g.2606514C>A , CM000673.1:g.2606514C>A	GRCh37
NC_000011.8:g.2563090C>A	NCBI36
NG_008935.1:g.145294C>A , LRG_287:g.145294C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.771+1739C>A	ENSP00000434560.2:n.771+1739C>A
ENST00000646564.2:c.588+1739C>A	ENSP00000495806.2:n.588+1739C>A
ENST00000155840.12:c.1105C>A MANE Select	ENSP00000155840.2:p.Pro369Thr
ENST00000335475.6:c.724C>A	ENSP00000334497.5:p.Pro242Thr
ENST00000646564.1:c.234+1739C>A	ENSP00000495806.1:n.234+1739C>A
ENST00000155840.9:c.1105C>A	ENSP00000155840.2:p.Pro369Thr
ENST00000335475.5:c.724C>A	ENSP00000334497.5:p.Pro242Thr
NM_000218.2:c.1105C>A , LRG_287t1:c.1105C>A	NP_000209.2:p.Pro369Thr
NM_181798.1:c.724C>A , LRG_287t2:c.724C>A	NP_861463.1:p.Pro242Thr
NM_000218.3:c.1105C>A MANE Select	NP_000209.2:p.Pro369Thr