Canonical Allele Identifier: CA951176046
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101764920_101764921insTTTTT , CM000674.2:g.101764920_101764921insTTTTT GRCh38
NC_000012.11:g.102158698_102158699insTTTTT , CM000674.1:g.102158698_102158699insTTTTT GRCh37
NC_000012.10:g.100682829_100682830insTTTTT NCBI36
NG_021243.1:g.70947_70948insAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.1996_1997insAAAAA MANE Select ENSP00000299314.7:p.Phe666Ter
ENST00000299314.11:c.1996_1997insAAAAA ENSP00000299314.7:p.Phe666Ter
NM_024312.4:c.1996_1997insAAAAA NP_077288.2:p.Phe666Ter
XM_006719593.2:c.1996_1997insAAAAA XP_006719656.1:p.Phe666Ter
XM_011538731.1:c.1915_1916insAAAAA XP_011537033.1:p.Phe639Ter
XM_006719593.3:c.1996_1997insAAAAA XP_006719656.1:p.Phe666Ter
XM_011538731.2:c.1915_1916insAAAAA XP_011537033.1:p.Phe639Ter
XM_017019961.1:c.1780_1781insAAAAA XP_016875450.1:p.Phe594Ter
XM_017019962.2:c.769_770insAAAAA XP_016875451.1:p.Phe257Ter
NM_024312.5:c.1996_1997insAAAAA MANE Select NP_077288.2:p.Phe666Ter