Canonical Allele Identifier: CA1190742520
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768439C= , CM000663.2:g.115768439C= GRCh38
NC_000001.10:g.116311060C= , CM000663.1:g.116311060C= GRCh37
NC_000001.9:g.116112583C= NCBI36
NG_008802.1:g.5367G= , LRG_404:g.5367G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-174G= ENSP00000518226.1:n.-174G=
ENST00000261448.6:c.103G= MANE Select ENSP00000261448.5:p.Val35=
ENST00000261448.5:c.103G= ENSP00000261448.5:p.Val35=
NM_001232.3:c.103G= , LRG_404t1:c.103G= NP_001223.2:p.Val35=
NM_001232.4:c.103G= MANE Select NP_001223.2:p.Val35=