Canonical Allele Identifier: CA2620445362

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101785860-AAATAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101785865_101785869del , CM000674.2:g.101785865_101785869del	GRCh38
NC_000012.11:g.102179643_102179647del , CM000674.1:g.102179643_102179647del	GRCh37
NC_000012.10:g.100703774_100703778del	NCBI36
NG_021243.1:g.50003_50007del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.571+147_571+151del MANE Select	ENSP00000299314.7:n.571+147_571+151del
ENST00000299314.11:c.571+147_571+151del	ENSP00000299314.7:n.571+147_571+151del
ENST00000549940.5:c.571+147_571+151del	ENSP00000449150.1:n.571+147_571+151del
ENST00000550352.1:n.512_516del
ENST00000552681.1:c.205+147_205+151del	ENSP00000449217.1:n.205+147_205+151del
NM_024312.4:c.571+147_571+151del	NP_077288.2:n.571+147_571+151del
XM_006719593.2:c.571+147_571+151del	XP_006719656.1:n.571+147_571+151del
XM_011538731.1:c.490+147_490+151del	XP_011537033.1:n.490+147_490+151del
XM_006719593.3:c.571+147_571+151del	XP_006719656.1:n.571+147_571+151del
XM_011538731.2:c.490+147_490+151del	XP_011537033.1:n.490+147_490+151del
XM_017019961.1:c.355+147_355+151del	XP_016875450.1:n.355+147_355+151del
XM_017019962.2:c.-780+147_-780+151del	XP_016875451.1:n.-780+147_-780+151del
NM_024312.5:c.571+147_571+151del MANE Select	NP_077288.2:n.571+147_571+151del