Canonical Allele Identifier: CA2635584912

Gene: ENO3

Linked Data

• gnomAD v4: 17-4955383-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955384_4955385del , CM000679.2:g.4955384_4955385del	GRCh38
NC_000017.10:g.4858679_4858680del , CM000679.1:g.4858679_4858680del	GRCh37
NC_000017.9:g.4799425_4799426del	NCBI36
NG_012063.2:g.14294_14295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.668-23_668-22del MANE Select	ENSP00000430055.2:n.668-23_668-22del
ENST00000323997.10:c.668-23_668-22del	ENSP00000324105.6:n.668-23_668-22del
ENST00000518175.1:c.668-23_668-22del	ENSP00000431087.1:n.668-23_668-22del
ENST00000519584.5:c.539-23_539-22del	ENSP00000430636.1:n.539-23_539-22del
ENST00000519602.5:c.668-23_668-22del	ENSP00000430055.1:n.668-23_668-22del
ENST00000521659.5:c.*614-23_*614-22del	ENSP00000430554.1:n.*614-23_*614-22del
NM_001193503.1:c.539-23_539-22del	NP_001180432.1:n.539-23_539-22del
NM_001976.4:c.668-23_668-22del	NP_001967.3:n.668-23_668-22del
NM_053013.3:c.668-23_668-22del	NP_443739.3:n.668-23_668-22del
XM_005256521.2:c.695-23_695-22del	XP_005256578.1:n.695-23_695-22del
XM_011523729.1:c.668-23_668-22del	XP_011522031.1:n.668-23_668-22del
XM_017024346.2:c.668-23_668-22del	XP_016879835.1:n.668-23_668-22del
NM_001193503.2:c.539-23_539-22del	NP_001180432.1:n.539-23_539-22del
NM_001374523.1:c.668-23_668-22del	NP_001361452.1:n.668-23_668-22del
NM_001374524.1:c.695-23_695-22del	NP_001361453.1:n.695-23_695-22del
NM_001976.5:c.668-23_668-22del	NP_001967.3:n.668-23_668-22del
NM_053013.4:c.668-23_668-22del MANE Select	NP_443739.3:n.668-23_668-22del