Canonical Allele Identifier: CA386305007

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179902G>C (hg19) ; chr12:g.101786124G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786124G>C , CM000674.2:g.101786124G>C	GRCh38
NC_000012.11:g.102179902G>C , CM000674.1:g.102179902G>C	GRCh37
NC_000012.10:g.100704033G>C	NCBI36
NG_021243.1:g.49744C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.459C>G MANE Select	ENSP00000299314.7:p.Asp153Glu
ENST00000299314.11:c.459C>G	ENSP00000299314.7:p.Asp153Glu
ENST00000549940.5:c.459C>G	ENSP00000449150.1:p.Asp153Glu
ENST00000550352.1:n.253C>G
ENST00000552681.1:c.93C>G	ENSP00000449217.1:p.Asp31Glu
NM_024312.4:c.459C>G	NP_077288.2:p.Asp153Glu
XM_006719593.2:c.459C>G	XP_006719656.1:p.Asp153Glu
XM_011538731.1:c.378C>G	XP_011537033.1:p.Asp126Glu
XM_006719593.3:c.459C>G	XP_006719656.1:p.Asp153Glu
XM_011538731.2:c.378C>G	XP_011537033.1:p.Asp126Glu
XM_017019961.1:c.243C>G	XP_016875450.1:p.Asp81Glu
XM_017019962.2:c.-892C>G	XP_016875451.1:n.-892C>G
NM_024312.5:c.459C>G MANE Select	NP_077288.2:p.Asp153Glu