Canonical Allele Identifier: CA497679499

Gene: ENO3

Linked Data

• ClinVar Variation Id: 2808625
• ClinVar RCV Id: RCV003631627
• MyVariant Identifiers: chr17:g.4858721G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955426G>C , CM000679.2:g.4955426G>C	GRCh38
NC_000017.10:g.4858721G>C , CM000679.1:g.4858721G>C	GRCh37
NC_000017.9:g.4799467G>C	NCBI36
NG_012063.2:g.14336G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.687G>C MANE Select	ENSP00000430055.2:p.Thr229=
ENST00000323997.10:c.687G>C	ENSP00000324105.6:p.Thr229=
ENST00000518175.1:c.687G>C	ENSP00000431087.1:p.Thr229=
ENST00000519584.5:c.558G>C	ENSP00000430636.1:p.Thr186=
ENST00000519602.5:c.687G>C	ENSP00000430055.1:p.Thr229=
ENST00000521659.5:c.*633G>C	ENSP00000430554.1:n.*633G>C
NM_001193503.1:c.558G>C	NP_001180432.1:p.Thr186=
NM_001976.4:c.687G>C	NP_001967.3:p.Thr229=
NM_053013.3:c.687G>C	NP_443739.3:p.Thr229=
XM_005256521.2:c.714G>C	XP_005256578.1:p.Thr238=
XM_011523729.1:c.687G>C	XP_011522031.1:p.Thr229=
XM_017024346.2:c.687G>C	XP_016879835.1:p.Thr229=
NM_001193503.2:c.558G>C	NP_001180432.1:p.Thr186=
NM_001374523.1:c.687G>C	NP_001361452.1:p.Thr229=
NM_001374524.1:c.714G>C	NP_001361453.1:p.Thr238=
NM_001976.5:c.687G>C	NP_001967.3:p.Thr229=
NM_053013.4:c.687G>C MANE Select	NP_443739.3:p.Thr229=