Canonical Allele Identifier: CA2058958040

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770579G= , CM000674.2:g.101770579G=	GRCh38
NC_000012.11:g.102164357G= , CM000674.1:g.102164357G=	GRCh37
NC_000012.10:g.100688488G=	NCBI36
NG_021243.1:g.65289C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.940C= MANE Select	ENSP00000299314.7:p.Gln314=
ENST00000299314.11:c.940C=	ENSP00000299314.7:p.Gln314=
ENST00000549940.5:c.940C=	ENSP00000449150.1:p.Gln314=
NM_024312.4:c.940C=	NP_077288.2:p.Gln314=
XM_006719593.2:c.940C=	XP_006719656.1:p.Gln314=
XM_011538731.1:c.859C=	XP_011537033.1:p.Gln287=
XM_006719593.3:c.940C=	XP_006719656.1:p.Gln314=
XM_011538731.2:c.859C=	XP_011537033.1:p.Gln287=
XM_017019961.1:c.724C=	XP_016875450.1:p.Gln242=
XM_017019962.2:c.-288C=	XP_016875451.1:n.-288C=
NM_024312.5:c.940C= MANE Select	NP_077288.2:p.Gln314=