Canonical Allele Identifier: CA413207720
Gene: GSPT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.51487753T>A (hg19) chrX:g.51744657T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.51744657T>A , CM000685.2:g.51744657T>A GRCh38
NC_000023.10:g.51487753T>A , CM000685.1:g.51487753T>A GRCh37
NC_000023.9:g.51504493T>A NCBI36
NG_016857.1:g.6273T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340438.6:c.1031T>A MANE Select ENSP00000341247.4:p.Leu344Ter
ENST00000340438.5:c.1031T>A ENSP00000341247.4:p.Leu344Ter
NM_018094.4:c.1031T>A NP_060564.2:p.Leu344Ter
NM_018094.5:c.1031T>A MANE Select NP_060564.2:p.Leu344Ter
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Search 100 bp 3'