Canonical Allele Identifier: CA394186757

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1361877_1361882del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361880_1361885del , CM000678.2:g.1361880_1361885del	GRCh38
NC_000016.9:g.1411881_1411886del , CM000678.1:g.1411881_1411886del	GRCh37
NC_000016.8:g.1351882_1351887del	NCBI36
NG_016985.1:g.14982_14987del
NG_033129.1:g.57823_57828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.341_346del
ENST00000529110.2:c.326_331del	ENSP00000435349.2:p.Tyr109_Glu110del
ENST00000529957.6:n.300_305del
ENST00000683366.1:c.187_192del	ENSP00000507283.1:p.Met63_Ser64del
ENST00000683887.1:c.290_295del	ENSP00000506886.1:p.Tyr97_Glu98del
ENST00000684100.1:n.236_241del
ENST00000684126.1:n.300_305del
ENST00000684688.1:n.867_872del
ENST00000204679.9:c.242_247del MANE Select	ENSP00000204679.4:p.Tyr81_Glu82del
ENST00000204679.8:c.242_247del	ENSP00000204679.4:p.Tyr81_Glu82del
ENST00000526820.5:c.*144_*149del	ENSP00000434413.1:n.*144_*149del
ENST00000527076.1:n.1258_1263del
ENST00000527168.5:n.278_283del
ENST00000529110.1:c.309_314del
ENST00000529957.5:n.341_346del
NM_032520.4:c.242_247del	NP_115909.1:p.Tyr81_Glu82del
XM_017023782.1:c.290_295del	XP_016879271.1:p.Tyr97_Glu98del
XM_017023783.1:c.-119_-114del	XP_016879272.1:n.-119_-114del
NM_032520.5:c.242_247del MANE Select	NP_115909.1:p.Tyr81_Glu82del