Canonical Allele Identifier: CA386301995
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101768118G>C , CM000674.2:g.101768118G>C GRCh38
NC_000012.11:g.102161896G>C , CM000674.1:g.102161896G>C GRCh37
NC_000012.10:g.100686027G>C NCBI36
NG_021243.1:g.67750C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.1327C>G MANE Select ENSP00000299314.7:p.Pro443Ala
ENST00000299314.11:c.1327C>G ENSP00000299314.7:p.Pro443Ala
ENST00000549940.5:c.1327C>G ENSP00000449150.1:p.Pro443Ala
NM_024312.4:c.1327C>G NP_077288.2:p.Pro443Ala
XM_006719593.2:c.1327C>G XP_006719656.1:p.Pro443Ala
XM_011538731.1:c.1246C>G XP_011537033.1:p.Pro416Ala
XM_006719593.3:c.1327C>G XP_006719656.1:p.Pro443Ala
XM_011538731.2:c.1246C>G XP_011537033.1:p.Pro416Ala
XM_017019961.1:c.1111C>G XP_016875450.1:p.Pro371Ala
XM_017019962.2:c.100C>G XP_016875451.1:p.Pro34Ala
NM_024312.5:c.1327C>G MANE Select NP_077288.2:p.Pro443Ala