Canonical Allele Identifier: CA2635584334
Gene: ENO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4955010_4955011insA , CM000679.2:g.4955010_4955011insA GRCh38
NC_000017.10:g.4858305_4858306insA , CM000679.1:g.4858305_4858306insA GRCh37
NC_000017.9:g.4799051_4799052insA NCBI36
NG_012063.2:g.13920_13921insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000519602.6:c.445-65_445-64insA MANE Select ENSP00000430055.2:n.445-65_445-64insA
ENST00000323997.10:c.445-65_445-64insA ENSP00000324105.6:n.445-65_445-64insA
ENST00000518175.1:c.445-65_445-64insA ENSP00000431087.1:n.445-65_445-64insA
ENST00000519584.5:c.316-65_316-64insA ENSP00000430636.1:n.316-65_316-64insA
ENST00000519602.5:c.445-65_445-64insA ENSP00000430055.1:n.445-65_445-64insA
ENST00000520221.5:c.445-65_445-64insA ENSP00000467444.1:n.445-65_445-64insA
ENST00000521659.5:c.*391-65_*391-64insA ENSP00000430554.1:n.*391-65_*391-64insA
ENST00000522249.5:c.445-65_445-64insA ENSP00000428811.1:n.445-65_445-64insA
ENST00000522301.5:c.445-65_445-64insA ENSP00000465697.1:n.445-65_445-64insA
NM_001193503.1:c.316-65_316-64insA NP_001180432.1:n.316-65_316-64insA
NM_001976.4:c.445-65_445-64insA NP_001967.3:n.445-65_445-64insA
NM_053013.3:c.445-65_445-64insA NP_443739.3:n.445-65_445-64insA
XM_005256521.2:c.472-65_472-64insA XP_005256578.1:n.472-65_472-64insA
XM_011523729.1:c.445-65_445-64insA XP_011522031.1:n.445-65_445-64insA
XM_017024346.2:c.445-65_445-64insA XP_016879835.1:n.445-65_445-64insA
NM_001193503.2:c.316-65_316-64insA NP_001180432.1:n.316-65_316-64insA
NM_001374523.1:c.445-65_445-64insA NP_001361452.1:n.445-65_445-64insA
NM_001374524.1:c.472-65_472-64insA NP_001361453.1:n.472-65_472-64insA
NM_001976.5:c.445-65_445-64insA NP_001967.3:n.445-65_445-64insA
NM_053013.4:c.445-65_445-64insA MANE Select NP_443739.3:n.445-65_445-64insA