Canonical Allele Identifier: CA386304902

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179853C>G (hg19) ; chr12:g.101786075C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786075C>G , CM000674.2:g.101786075C>G	GRCh38
NC_000012.11:g.102179853C>G , CM000674.1:g.102179853C>G	GRCh37
NC_000012.10:g.100703984C>G	NCBI36
NG_021243.1:g.49793G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.508G>C MANE Select	ENSP00000299314.7:p.Val170Leu
ENST00000299314.11:c.508G>C	ENSP00000299314.7:p.Val170Leu
ENST00000549940.5:c.508G>C	ENSP00000449150.1:p.Val170Leu
ENST00000550352.1:n.302G>C
ENST00000552681.1:c.142G>C	ENSP00000449217.1:p.Val48Leu
NM_024312.4:c.508G>C	NP_077288.2:p.Val170Leu
XM_006719593.2:c.508G>C	XP_006719656.1:p.Val170Leu
XM_011538731.1:c.427G>C	XP_011537033.1:p.Val143Leu
XM_006719593.3:c.508G>C	XP_006719656.1:p.Val170Leu
XM_011538731.2:c.427G>C	XP_011537033.1:p.Val143Leu
XM_017019961.1:c.292G>C	XP_016875450.1:p.Val98Leu
XM_017019962.2:c.-843G>C	XP_016875451.1:n.-843G>C
NM_024312.5:c.508G>C MANE Select	NP_077288.2:p.Val170Leu