Canonical Allele Identifier: CA413207484
Gene: GSPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.51744555T>A , CM000685.2:g.51744555T>A GRCh38
NC_000023.10:g.51487651T>A , CM000685.1:g.51487651T>A GRCh37
NC_000023.9:g.51504391T>A NCBI36
NG_016857.1:g.6171T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340438.6:c.929T>A MANE Select ENSP00000341247.4:p.Leu310Gln
ENST00000340438.5:c.929T>A ENSP00000341247.4:p.Leu310Gln
NM_018094.4:c.929T>A NP_060564.2:p.Leu310Gln
NM_018094.5:c.929T>A MANE Select NP_060564.2:p.Leu310Gln