Canonical Allele Identifier: CA394187657

Gene: GNPTG

Linked Data

• gnomAD v4: 16-1362224-A-G
• MyVariant Identifiers: chr16:g.1412225A>G (hg19) ; chr16:g.1362224A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362224A>G , CM000678.2:g.1362224A>G	GRCh38
NC_000016.9:g.1412225A>G , CM000678.1:g.1412225A>G	GRCh37
NC_000016.8:g.1352226A>G	NCBI36
NG_016985.1:g.15326A>G
NG_033129.1:g.57481T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.529A>G
ENST00000529110.2:c.514A>G	ENSP00000435349.2:p.Lys172Glu
ENST00000529957.6:n.488A>G
ENST00000683366.1:c.*162A>G	ENSP00000507283.1:n.*162A>G
ENST00000683887.1:c.478A>G	ENSP00000506886.1:p.Lys160Glu
ENST00000684100.1:n.424A>G
ENST00000684126.1:n.488A>G
ENST00000684688.1:n.1055A>G
ENST00000204679.9:c.430A>G MANE Select	ENSP00000204679.4:p.Lys144Glu
ENST00000204679.8:c.430A>G	ENSP00000204679.4:p.Lys144Glu
ENST00000527076.1:n.1446A>G
ENST00000527168.5:n.466A>G
ENST00000529110.1:c.497A>G
ENST00000529957.5:n.529A>G
NM_032520.4:c.430A>G	NP_115909.1:p.Lys144Glu
XM_017023782.1:c.478A>G	XP_016879271.1:p.Lys160Glu
XM_017023783.1:c.70A>G	XP_016879272.1:p.Lys24Glu
NM_032520.5:c.430A>G MANE Select	NP_115909.1:p.Lys144Glu