Canonical Allele Identifier: CA341766977
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768318A>C , CM000663.2:g.115768318A>C GRCh38
NC_000001.10:g.116310939A>C , CM000663.1:g.116310939A>C GRCh37
NC_000001.9:g.116112462A>C NCBI36
NG_008802.1:g.5488T>G , LRG_404:g.5488T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-53T>G ENSP00000518226.1:n.-53T>G
ENST00000261448.6:c.224T>G MANE Select ENSP00000261448.5:p.Ile75Ser
ENST00000261448.5:c.224T>G ENSP00000261448.5:p.Ile75Ser
NM_001232.3:c.224T>G , LRG_404t1:c.224T>G NP_001223.2:p.Ile75Ser
NM_001232.4:c.224T>G MANE Select NP_001223.2:p.Ile75Ser