Canonical Allele Identifier: CA341763839

Gene: CASQ2

Linked Data

• MyVariant Identifiers: chr1:g.116280871C>A (hg19) ; chr1:g.115738250C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115738250C>A , CM000663.2:g.115738250C>A	GRCh38
NC_000001.10:g.116280871C>A , CM000663.1:g.116280871C>A	GRCh37
NC_000001.9:g.116082394C>A	NCBI36
NG_008802.1:g.35556G>T , LRG_404:g.35556G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488931.2:c.230G>T	ENSP00000518226.1:p.Gly77Val
ENST00000261448.6:c.506G>T MANE Select	ENSP00000261448.5:p.Gly169Val
ENST00000261448.5:c.506G>T	ENSP00000261448.5:p.Gly169Val
NM_001232.3:c.506G>T , LRG_404t1:c.506G>T	NP_001223.2:p.Gly169Val
NM_001232.4:c.506G>T MANE Select	NP_001223.2:p.Gly169Val