Canonical Allele Identifier: CA338099445
Gene: ESPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6451926A>G , CM000663.2:g.6451926A>G GRCh38
NC_000001.10:g.6511986A>G , CM000663.1:g.6511986A>G GRCh37
NC_000001.9:g.6434573A>G NCBI36
NG_015866.1:g.32139A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000434576.2:c.185A>G
ENST00000461727.6:c.457A>G ENSP00000465308.1:p.Ser153Gly
ENST00000475228.6:c.223A>G ENSP00000488721.2:p.Ser75Gly
ENST00000477679.2:c.210A>G
ENST00000636330.1:c.2155A>G ENSP00000490186.1:p.Ser719Gly
ENST00000636644.1:c.280A>G ENSP00000490230.1:p.Ser94Gly
ENST00000645284.1:c.2155A>G MANE Select ENSP00000496593.1:p.Ser719Gly
ENST00000377828.5:c.2155A>G ENSP00000367059.1:p.Ser719Gly
ENST00000416731.5:c.457A>G ENSP00000399239.2:p.Ser153Gly
ENST00000434576.1:c.185A>G
ENST00000461727.5:c.457A>G ENSP00000465308.1:p.Ser153Gly
ENST00000475228.5:c.220A>G ENSP00000488721.1:p.Ser74Gly
ENST00000475479.2:n.337A>G
ENST00000477679.1:n.210A>G
ENST00000633239.1:c.304A>G ENSP00000488071.1:p.Ser102Gly
NM_031475.2:c.2155A>G NP_113663.2:p.Ser719Gly
XM_005263501.2:c.2092A>G XP_005263558.1:p.Ser698Gly
XM_011542231.1:c.2092A>G XP_011540533.1:p.Ser698Gly
XM_011542232.1:c.2065A>G XP_011540534.1:p.Ser689Gly
XM_011542233.1:c.1696A>G XP_011540535.1:p.Ser566Gly
XM_011542234.1:c.1033A>G XP_011540536.1:p.Ser345Gly
XM_011542235.1:c.2065A>G XP_011540537.1:p.Ser689Gly
XM_011542236.1:c.280A>G XP_011540538.1:p.Ser94Gly
NM_031475.3:c.2155A>G MANE Select NP_113663.2:p.Ser719Gly
XM_011542233.2:c.1696A>G XP_011540535.1:p.Ser566Gly
XM_011542236.2:c.280A>G XP_011540538.1:p.Ser94Gly
XM_017002433.1:c.2092A>G XP_016857922.1:p.Ser698Gly
XM_024450116.1:c.2065A>G XP_024305884.1:p.Ser689Gly
NM_001367473.1:c.2065A>G NP_001354402.1:p.Ser689Gly
NM_001367474.1:c.2092A>G NP_001354403.1:p.Ser698Gly