Canonical Allele Identifier: CA2620444777

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101785526-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101785529_101785530del , CM000674.2:g.101785529_101785530del	GRCh38
NC_000012.11:g.102179307_102179308del , CM000674.1:g.102179307_102179308del	GRCh37
NC_000012.10:g.100703438_100703439del	NCBI36
NG_021243.1:g.50340_50341del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.571+484_571+485del MANE Select	ENSP00000299314.7:n.571+484_571+485del
ENST00000299314.11:c.571+484_571+485del	ENSP00000299314.7:n.571+484_571+485del
ENST00000549940.5:c.571+484_571+485del	ENSP00000449150.1:n.571+484_571+485del
ENST00000552681.1:c.205+484_205+485del	ENSP00000449217.1:n.205+484_205+485del
NM_024312.4:c.571+484_571+485del	NP_077288.2:n.571+484_571+485del
XM_006719593.2:c.571+484_571+485del	XP_006719656.1:n.571+484_571+485del
XM_011538731.1:c.490+484_490+485del	XP_011537033.1:n.490+484_490+485del
XM_006719593.3:c.571+484_571+485del	XP_006719656.1:n.571+484_571+485del
XM_011538731.2:c.490+484_490+485del	XP_011537033.1:n.490+484_490+485del
XM_017019961.1:c.355+484_355+485del	XP_016875450.1:n.355+484_355+485del
XM_017019962.2:c.-780+484_-780+485del	XP_016875451.1:n.-780+484_-780+485del
NM_024312.5:c.571+484_571+485del MANE Select	NP_077288.2:n.571+484_571+485del