Canonical Allele Identifier: CA2058950619
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753561G= , CM000674.2:g.101753561G= GRCh38
NC_000012.11:g.102147339G= , CM000674.1:g.102147339G= GRCh37
NC_000012.10:g.100671470G= NCBI36
NG_021243.1:g.82307C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.3435-22C= MANE Select ENSP00000299314.7:n.3435-22C=
ENST00000299314.11:c.3435-22C= ENSP00000299314.7:n.3435-22C=
ENST00000549738.5:c.333-22C= ENSP00000450161.1:n.333-22C=
NM_024312.4:c.3435-22C= NP_077288.2:n.3435-22C=
XM_011538731.1:c.3354-22C= XP_011537033.1:n.3354-22C=
XM_011538731.2:c.3354-22C= XP_011537033.1:n.3354-22C=
XM_017019961.1:c.3219-22C= XP_016875450.1:n.3219-22C=
XM_017019962.2:c.2208-22C= XP_016875451.1:n.2208-22C=
NM_024312.5:c.3435-22C= MANE Select NP_077288.2:n.3435-22C=