Canonical Allele Identifier: CA2058950620
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753566T= , CM000674.2:g.101753566T= GRCh38
NC_000012.11:g.102147344T= , CM000674.1:g.102147344T= GRCh37
NC_000012.10:g.100671475T= NCBI36
NG_021243.1:g.82302A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.3435-27A= MANE Select ENSP00000299314.7:n.3435-27A=
ENST00000299314.11:c.3435-27A= ENSP00000299314.7:n.3435-27A=
ENST00000549738.5:c.333-27A= ENSP00000450161.1:n.333-27A=
NM_024312.4:c.3435-27A= NP_077288.2:n.3435-27A=
XM_011538731.1:c.3354-27A= XP_011537033.1:n.3354-27A=
XM_011538731.2:c.3354-27A= XP_011537033.1:n.3354-27A=
XM_017019961.1:c.3219-27A= XP_016875450.1:n.3219-27A=
XM_017019962.2:c.2208-27A= XP_016875451.1:n.2208-27A=
NM_024312.5:c.3435-27A= MANE Select NP_077288.2:n.3435-27A=