Canonical Allele Identifier: CA2058985249

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830772C= , CM000674.2:g.101830772C=	GRCh38
NC_000012.11:g.102224550C= , CM000674.1:g.102224550C=	GRCh37
NC_000012.10:g.100748681C=	NCBI36
NG_021243.1:g.5096G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.-97G= MANE Select	ENSP00000299314.7:n.-97G=
ENST00000299314.11:c.-97G=	ENSP00000299314.7:n.-97G=
ENST00000392919.4:c.-97G=	ENSP00000376651.4:n.-97G=
ENST00000549940.5:c.-97G=	ENSP00000449150.1:n.-97G=
NM_024312.4:c.-97G=	NP_077288.2:n.-97G=
XM_006719593.2:c.-97G=	XP_006719656.1:n.-97G=
XM_006719593.3:c.-97G=	XP_006719656.1:n.-97G=
XM_017019961.1:c.-246G=	XP_016875450.1:n.-246G=
XM_017019962.2:c.-1447G=	XP_016875451.1:n.-1447G=
NM_024312.5:c.-97G= MANE Select	NP_077288.2:n.-97G=