Canonical Allele Identifier: CA386304776
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101786014T>G , CM000674.2:g.101786014T>G GRCh38
NC_000012.11:g.102179792T>G , CM000674.1:g.102179792T>G GRCh37
NC_000012.10:g.100703923T>G NCBI36
NG_021243.1:g.49854A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.569A>C MANE Select ENSP00000299314.7:p.Asp190Ala
ENST00000299314.11:c.569A>C ENSP00000299314.7:p.Asp190Ala
ENST00000549940.5:c.569A>C ENSP00000449150.1:p.Asp190Ala
ENST00000550352.1:n.363A>C
ENST00000552681.1:c.203A>C ENSP00000449217.1:p.Asp68Ala
NM_024312.4:c.569A>C NP_077288.2:p.Asp190Ala
XM_006719593.2:c.569A>C XP_006719656.1:p.Asp190Ala
XM_011538731.1:c.488A>C XP_011537033.1:p.Asp163Ala
XM_006719593.3:c.569A>C XP_006719656.1:p.Asp190Ala
XM_011538731.2:c.488A>C XP_011537033.1:p.Asp163Ala
XM_017019961.1:c.353A>C XP_016875450.1:p.Asp118Ala
XM_017019962.2:c.-782A>C XP_016875451.1:n.-782A>C
NM_024312.5:c.569A>C MANE Select NP_077288.2:p.Asp190Ala