Canonical Allele Identifier: CA2058950592

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101753504T= , CM000674.2:g.101753504T=	GRCh38
NC_000012.11:g.102147282T= , CM000674.1:g.102147282T=	GRCh37
NC_000012.10:g.100671413T=	NCBI36
NG_021243.1:g.82364A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3470A= MANE Select	ENSP00000299314.7:p.Asn1157=
ENST00000299314.11:c.3470A=	ENSP00000299314.7:p.Asn1157=
ENST00000549738.5:c.368A=	ENSP00000450161.1:n.368A=
NM_024312.4:c.3470A=	NP_077288.2:p.Asn1157=
XM_011538731.1:c.3389A=	XP_011537033.1:p.Asn1130=
XM_011538731.2:c.3389A=	XP_011537033.1:p.Asn1130=
XM_017019961.1:c.3254A=	XP_016875450.1:p.Asn1085=
XM_017019962.2:c.2243A=	XP_016875451.1:p.Asn748=
NM_024312.5:c.3470A= MANE Select	NP_077288.2:p.Asn1157=