Canonical Allele Identifier: CA341764005

Gene: CASQ2

Linked Data

• MyVariant Identifiers: chr1:g.116280949T>A (hg19) ; chr1:g.115738328T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115738328T>A , CM000663.2:g.115738328T>A	GRCh38
NC_000001.10:g.116280949T>A , CM000663.1:g.116280949T>A	GRCh37
NC_000001.9:g.116082472T>A	NCBI36
NG_008802.1:g.35478A>T , LRG_404:g.35478A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488931.2:c.152A>T	ENSP00000518226.1:p.Glu51Val
ENST00000261448.6:c.428A>T MANE Select	ENSP00000261448.5:p.Glu143Val
ENST00000261448.5:c.428A>T	ENSP00000261448.5:p.Glu143Val
NM_001232.3:c.428A>T , LRG_404t1:c.428A>T	NP_001223.2:p.Glu143Val
NM_001232.4:c.428A>T MANE Select	NP_001223.2:p.Glu143Val