Canonical Allele Identifier: CA341767329

Gene: CASQ2

Linked Data

• MyVariant Identifiers: chr1:g.116311093T>A (hg19) ; chr1:g.115768472T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115768472T>A , CM000663.2:g.115768472T>A	GRCh38
NC_000001.10:g.116311093T>A , CM000663.1:g.116311093T>A	GRCh37
NC_000001.9:g.116112616T>A	NCBI36
NG_008802.1:g.5334A>T , LRG_404:g.5334A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488931.2:c.-207A>T	ENSP00000518226.1:n.-207A>T
ENST00000261448.6:c.70A>T MANE Select	ENSP00000261448.5:p.Asn24Tyr
ENST00000261448.5:c.70A>T	ENSP00000261448.5:p.Asn24Tyr
NM_001232.3:c.70A>T , LRG_404t1:c.70A>T	NP_001223.2:p.Asn24Tyr
NM_001232.4:c.70A>T MANE Select	NP_001223.2:p.Asn24Tyr