Canonical Allele Identifier: CA2058952147
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101757147C= , CM000674.2:g.101757147C= GRCh38
NC_000012.11:g.102150925C= , CM000674.1:g.102150925C= GRCh37
NC_000012.10:g.100675056C= NCBI36
NG_021243.1:g.78721G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.3434+65G= MANE Select ENSP00000299314.7:n.3434+65G=
ENST00000299314.11:c.3434+65G= ENSP00000299314.7:n.3434+65G=
ENST00000549194.1:n.365G=
ENST00000549738.5:c.185+65G= ENSP00000450161.1:n.185+65G=
ENST00000550718.1:c.246+65G=
NM_024312.4:c.3434+65G= NP_077288.2:n.3434+65G=
XM_006719593.2:c.3434+65G= XP_006719656.1:n.3434+65G=
XM_011538731.1:c.3353+65G= XP_011537033.1:n.3353+65G=
XM_006719593.3:c.3434+65G= XP_006719656.1:n.3434+65G=
XM_011538731.2:c.3353+65G= XP_011537033.1:n.3353+65G=
XM_017019961.1:c.3218+65G= XP_016875450.1:n.3218+65G=
XM_017019962.2:c.2207+65G= XP_016875451.1:n.2207+65G=
NM_024312.5:c.3434+65G= MANE Select NP_077288.2:n.3434+65G=