Canonical Allele Identifier: CA2058985171

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830658C= , CM000674.2:g.101830658C=	GRCh38
NC_000012.11:g.102224436C= , CM000674.1:g.102224436C=	GRCh37
NC_000012.10:g.100748567C=	NCBI36
NG_021243.1:g.5210G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.18G= MANE Select	ENSP00000299314.7:p.Leu6=
ENST00000647144.1:n.6G=
ENST00000299314.11:c.18G=	ENSP00000299314.7:p.Leu6=
ENST00000392919.4:c.18G=	ENSP00000376651.4:p.Leu6=
ENST00000549165.1:c.18G=	ENSP00000450413.1:p.Leu6=
ENST00000549940.5:c.18G=	ENSP00000449150.1:p.Leu6=
NM_024312.4:c.18G=	NP_077288.2:p.Leu6=
XM_006719593.2:c.18G=	XP_006719656.1:p.Leu6=
XM_006719593.3:c.18G=	XP_006719656.1:p.Leu6=
XM_017019961.1:c.-132G=	XP_016875450.1:n.-132G=
XM_017019962.2:c.-1333G=	XP_016875451.1:n.-1333G=
NM_024312.5:c.18G= MANE Select	NP_077288.2:p.Leu6=