Canonical Allele Identifier: CA2058956979

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101768082C= , CM000674.2:g.101768082C=	GRCh38
NC_000012.11:g.102161860C= , CM000674.1:g.102161860C=	GRCh37
NC_000012.10:g.100685991C=	NCBI36
NG_021243.1:g.67786G=

Transcript Alleles

HGVS	Amino-acid Change
NM_024312.5:c.1363G= MANE Select	NP_077288.2:p.Ala455=
ENST00000299314.12:c.1363G= MANE Select	ENSP00000299314.7:p.Ala455=
NM_024312.4:c.1363G=	NP_077288.2:p.Ala455=
ENST00000299314.11:c.1363G=	ENSP00000299314.7:p.Ala455=
ENST00000549940.5:c.1363G=	ENSP00000449150.1:p.Ala455=
ENST00000552009.1:n.22G=
XM_006719593.2:c.1363G=	XP_006719656.1:p.Ala455=
XM_006719593.3:c.1363G=	XP_006719656.1:p.Ala455=
XM_011538731.1:c.1282G=	XP_011537033.1:p.Ala428=
XM_011538731.2:c.1282G=	XP_011537033.1:p.Ala428=
XM_017019961.1:c.1147G=	XP_016875450.1:p.Ala383=
XM_017019962.2:c.136G=	XP_016875451.1:p.Ala46=