Canonical Allele Identifier: CA386292240
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753410A>C , CM000674.2:g.101753410A>C GRCh38
NC_000012.11:g.102147188A>C , CM000674.1:g.102147188A>C GRCh37
NC_000012.10:g.100671319A>C NCBI36
NG_021243.1:g.82458T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.3564T>G MANE Select ENSP00000299314.7:p.Tyr1188Ter
ENST00000299314.11:c.3564T>G ENSP00000299314.7:p.Tyr1188Ter
ENST00000549738.5:c.462T>G ENSP00000450161.1:n.462T>G
NM_024312.4:c.3564T>G NP_077288.2:p.Tyr1188Ter
XM_011538731.1:c.3483T>G XP_011537033.1:p.Tyr1161Ter
XM_011538731.2:c.3483T>G XP_011537033.1:p.Tyr1161Ter
XM_017019961.1:c.3348T>G XP_016875450.1:p.Tyr1116Ter
XM_017019962.2:c.2337T>G XP_016875451.1:p.Tyr779Ter
NM_024312.5:c.3564T>G MANE Select NP_077288.2:p.Tyr1188Ter