Canonical Allele Identifier: CA2058952859

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761517C= , CM000674.2:g.101761517C=	GRCh38
NC_000012.11:g.102155295C= , CM000674.1:g.102155295C=	GRCh37
NC_000012.10:g.100679426C=	NCBI36
NG_021243.1:g.74351G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.2915+47G= MANE Select	ENSP00000299314.7:n.2915+47G=
ENST00000299314.11:c.2915+47G=	ENSP00000299314.7:n.2915+47G=
NM_024312.4:c.2915+47G=	NP_077288.2:n.2915+47G=
XM_006719593.2:c.2915+47G=	XP_006719656.1:n.2915+47G=
XM_011538731.1:c.2834+47G=	XP_011537033.1:n.2834+47G=
XM_006719593.3:c.2915+47G=	XP_006719656.1:n.2915+47G=
XM_011538731.2:c.2834+47G=	XP_011537033.1:n.2834+47G=
XM_017019961.1:c.2699+47G=	XP_016875450.1:n.2699+47G=
XM_017019962.2:c.1688+47G=	XP_016875451.1:n.1688+47G=
NM_024312.5:c.2915+47G= MANE Select	NP_077288.2:n.2915+47G=