Canonical Allele Identifier: CA2058985190

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830691A= , CM000674.2:g.101830691A=	GRCh38
NC_000012.11:g.102224469A= , CM000674.1:g.102224469A=	GRCh37
NC_000012.10:g.100748600A=	NCBI36
NG_021243.1:g.5177T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.-16T= MANE Select	ENSP00000299314.7:n.-16T=
ENST00000299314.11:c.-16T=	ENSP00000299314.7:n.-16T=
ENST00000392919.4:c.-16T=	ENSP00000376651.4:n.-16T=
ENST00000549940.5:c.-16T=	ENSP00000449150.1:n.-16T=
NM_024312.4:c.-16T=	NP_077288.2:n.-16T=
XM_006719593.2:c.-16T=	XP_006719656.1:n.-16T=
XM_006719593.3:c.-16T=	XP_006719656.1:n.-16T=
XM_017019961.1:c.-165T=	XP_016875450.1:n.-165T=
XM_017019962.2:c.-1366T=	XP_016875451.1:n.-1366T=
NM_024312.5:c.-16T= MANE Select	NP_077288.2:n.-16T=