Canonical Allele Identifier: CA341763850
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738256A>C , CM000663.2:g.115738256A>C GRCh38
NC_000001.10:g.116280877A>C , CM000663.1:g.116280877A>C GRCh37
NC_000001.9:g.116082400A>C NCBI36
NG_008802.1:g.35550T>G , LRG_404:g.35550T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.224T>G ENSP00000518226.1:p.Leu75Arg
ENST00000261448.6:c.500T>G MANE Select ENSP00000261448.5:p.Leu167Arg
ENST00000261448.5:c.500T>G ENSP00000261448.5:p.Leu167Arg
NM_001232.3:c.500T>G , LRG_404t1:c.500T>G NP_001223.2:p.Leu167Arg
NM_001232.4:c.500T>G MANE Select NP_001223.2:p.Leu167Arg