Canonical Allele Identifier: CA420178330

Gene: CASQ2

Linked Data

• MyVariant Identifiers: chr1:g.116310983C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115768362C>A , CM000663.2:g.115768362C>A	GRCh38
NC_000001.10:g.116310983C>A , CM000663.1:g.116310983C>A	GRCh37
NC_000001.9:g.116112506C>A	NCBI36
NG_008802.1:g.5444G>T , LRG_404:g.5444G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488931.2:c.-97G>T	ENSP00000518226.1:n.-97G>T
ENST00000261448.6:c.180G>T MANE Select	ENSP00000261448.5:p.Val60=
ENST00000261448.5:c.180G>T	ENSP00000261448.5:p.Val60=
NM_001232.3:c.180G>T , LRG_404t1:c.180G>T	NP_001223.2:p.Val60=
NM_001232.4:c.180G>T MANE Select	NP_001223.2:p.Val60=