Canonical Allele Identifier: CA2631583152

Gene: NAGPA

Linked Data

• gnomAD v4: 16-5027710-TGCAGGTGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5027713_5027721del , CM000678.2:g.5027713_5027721del	GRCh38
NC_000016.9:g.5077714_5077722del , CM000678.1:g.5077714_5077722del	GRCh37
NC_000016.8:g.5017715_5017723del	NCBI36
NG_028152.1:g.11223_11231del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1174+127_1174+135del MANE Select	ENSP00000310998.3:n.1174+127_1174+135del
ENST00000649828.1:c.*346+127_*346+135del	ENSP00000498032.1:n.*346+127_*346+135del
ENST00000312251.7:c.1174+127_1174+135del	ENSP00000310998.3:n.1174+127_1174+135del
ENST00000381955.7:c.1174+127_1174+135del	ENSP00000371381.3:n.1174+127_1174+135del
ENST00000562746.5:c.*346+127_*346+135del	ENSP00000455900.1:n.*346+127_*346+135del
ENST00000563578.5:c.738+1161_738+1169del
ENST00000564397.5:n.2227+127_2227+135del
ENST00000565876.5:c.481-340_481-332del
ENST00000566137.5:n.472+127_472+135del
ENST00000567739.5:n.493+127_493+135del
ENST00000568202.5:n.1037+127_1037+135del
ENST00000569296.5:c.787+127_787+135del	ENSP00000465949.1:n.787+127_787+135del
NM_016256.3:c.1174+127_1174+135del	NP_057340.2:n.1174+127_1174+135del
XM_011522517.1:c.1174+127_1174+135del	XP_011520819.1:n.1174+127_1174+135del
XR_243285.1:n.1270+127_1270+135del
XM_011522517.3:c.1174+127_1174+135del	XP_011520819.1:n.1174+127_1174+135del
XR_001751908.2:n.1269+127_1269+135del
XR_001751909.2:n.1273+127_1273+135del
XR_001751910.2:n.1302+127_1302+135del
XR_001751911.2:n.1302+127_1302+135del
XR_001751912.2:n.1306+127_1306+135del
NM_016256.4:c.1174+127_1174+135del MANE Select	NP_057340.2:n.1174+127_1174+135del