Canonical Allele Identifier: CA386304847

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179826T>C (hg19) ; chr12:g.101786048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786048T>C , CM000674.2:g.101786048T>C	GRCh38
NC_000012.11:g.102179826T>C , CM000674.1:g.102179826T>C	GRCh37
NC_000012.10:g.100703957T>C	NCBI36
NG_021243.1:g.49820A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.535A>G MANE Select	ENSP00000299314.7:p.Asn179Asp
ENST00000299314.11:c.535A>G	ENSP00000299314.7:p.Asn179Asp
ENST00000549940.5:c.535A>G	ENSP00000449150.1:p.Asn179Asp
ENST00000550352.1:n.329A>G
ENST00000552681.1:c.169A>G	ENSP00000449217.1:p.Asn57Asp
NM_024312.4:c.535A>G	NP_077288.2:p.Asn179Asp
XM_006719593.2:c.535A>G	XP_006719656.1:p.Asn179Asp
XM_011538731.1:c.454A>G	XP_011537033.1:p.Asn152Asp
XM_006719593.3:c.535A>G	XP_006719656.1:p.Asn179Asp
XM_011538731.2:c.454A>G	XP_011537033.1:p.Asn152Asp
XM_017019961.1:c.319A>G	XP_016875450.1:p.Asn107Asp
XM_017019962.2:c.-816A>G	XP_016875451.1:n.-816A>G
NM_024312.5:c.535A>G MANE Select	NP_077288.2:p.Asn179Asp