Canonical Allele Identifier: CA624856838

Gene: ENO3

Linked Data

• dbSNP Id: rs1356501653
• gnomAD v2: 17-4858603-AG-A
• gnomAD v3: 17-4955308-AG-A
• gnomAD v4: 17-4955308-AG-A
• MyVariant Identifiers: chr17:g.4858604del (hg19) ; chr17:g.4955309del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955309del , CM000679.2:g.4955309del	GRCh38
NC_000017.10:g.4858604del , CM000679.1:g.4858604del	GRCh37
NC_000017.9:g.4799350del	NCBI36
NG_012063.2:g.14219del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.667+12del MANE Select	ENSP00000430055.2:n.667+12del
ENST00000323997.10:c.667+12del	ENSP00000324105.6:n.667+12del
ENST00000518175.1:c.667+12del	ENSP00000431087.1:n.667+12del
ENST00000519584.5:c.538+12del	ENSP00000430636.1:n.538+12del
ENST00000519602.5:c.667+12del	ENSP00000430055.1:n.667+12del
ENST00000521659.5:c.*613+12del	ENSP00000430554.1:n.*613+12del
NM_001193503.1:c.538+12del	NP_001180432.1:n.538+12del
NM_001976.4:c.667+12del	NP_001967.3:n.667+12del
NM_053013.3:c.667+12del	NP_443739.3:n.667+12del
XM_005256521.2:c.694+12del	XP_005256578.1:n.694+12del
XM_011523729.1:c.667+12del	XP_011522031.1:n.667+12del
XM_017024346.2:c.667+12del	XP_016879835.1:n.667+12del
NM_001193503.2:c.538+12del	NP_001180432.1:n.538+12del
NM_001374523.1:c.667+12del	NP_001361452.1:n.667+12del
NM_001374524.1:c.694+12del	NP_001361453.1:n.694+12del
NM_001976.5:c.667+12del	NP_001967.3:n.667+12del
NM_053013.4:c.667+12del MANE Select	NP_443739.3:n.667+12del