Canonical Allele Identifier: CA341763835
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738247A>G , CM000663.2:g.115738247A>G GRCh38
NC_000001.10:g.116280868A>G , CM000663.1:g.116280868A>G GRCh37
NC_000001.9:g.116082391A>G NCBI36
NG_008802.1:g.35559T>C , LRG_404:g.35559T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.233T>C ENSP00000518226.1:p.Phe78Ser
ENST00000261448.6:c.509T>C MANE Select ENSP00000261448.5:p.Phe170Ser
ENST00000261448.5:c.509T>C ENSP00000261448.5:p.Phe170Ser
NM_001232.3:c.509T>C , LRG_404t1:c.509T>C NP_001223.2:p.Phe170Ser
NM_001232.4:c.509T>C MANE Select NP_001223.2:p.Phe170Ser