Canonical Allele Identifier: CA559979

Gene: ESPN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6440652C>G , CM000663.2:g.6440652C>G	GRCh38
NC_000001.10:g.6500712C>G , CM000663.1:g.6500712C>G	GRCh37
NC_000001.9:g.6423299C>G	NCBI36
NG_015866.1:g.20865C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636330.1:c.702C>G	ENSP00000490186.1:p.Ser234=
ENST00000645284.1:c.702C>G MANE Select	ENSP00000496593.1:p.Ser234=
ENST00000377828.5:c.702C>G	ENSP00000367059.1:p.Ser234=
ENST00000418286.1:c.64-7C>G	ENSP00000401793.1:n.64-7C>G
ENST00000632142.1:n.394C>G
ENST00000633651.1:n.421C>G
NM_031475.2:c.702C>G	NP_113663.2:p.Ser234=
XM_005263501.2:c.702C>G	XP_005263558.1:p.Ser234=
XM_011542231.1:c.702C>G	XP_011540533.1:p.Ser234=
XM_011542232.1:c.702C>G	XP_011540534.1:p.Ser234=
XM_011542233.1:c.306C>G	XP_011540535.1:p.Ser102=
XM_011542235.1:c.702C>G	XP_011540537.1:p.Ser234=
XM_011542237.1:c.702C>G	XP_011540539.1:p.Ser234=
XM_011542238.1:c.702C>G	XP_011540540.1:p.Ser234=
XR_946774.1:n.882C>G
XR_946775.1:n.882C>G
NM_031475.3:c.702C>G MANE Select	NP_113663.2:p.Ser234=
XM_011542233.2:c.306C>G	XP_011540535.1:p.Ser102=
XM_011542238.3:c.702C>G	XP_011540540.1:p.Ser234=
XM_017002433.1:c.702C>G	XP_016857922.1:p.Ser234=
XM_017002434.1:c.702C>G	XP_016857923.1:p.Ser234=
XM_024450116.1:c.702C>G	XP_024305884.1:p.Ser234=
NM_001367473.1:c.702C>G	NP_001354402.1:p.Ser234=
NM_001367474.1:c.702C>G	NP_001354403.1:p.Ser234=