Canonical Allele Identifier: CA17194290

Gene: ESPN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6428079dup , CM000663.2:g.6428079dup	GRCh38
NC_000001.10:g.6488139dup , CM000663.1:g.6488139dup	GRCh37
NC_000001.9:g.6410726dup	NCBI36
NG_015866.1:g.8292dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636330.1:c.295-147dup	ENSP00000490186.1:n.295-147dup
ENST00000645284.1:c.295-147dup MANE Select	ENSP00000496593.1:n.295-147dup
ENST00000377828.5:c.295-147dup	ENSP00000367059.1:n.295-147dup
NM_031475.2:c.295-147dup	NP_113663.2:n.295-147dup
XM_005263501.2:c.295-147dup	XP_005263558.1:n.295-147dup
XM_011542231.1:c.295-147dup	XP_011540533.1:n.295-147dup
XM_011542232.1:c.295-147dup	XP_011540534.1:n.295-147dup
XM_011542235.1:c.295-147dup	XP_011540537.1:n.295-147dup
XM_011542237.1:c.295-147dup	XP_011540539.1:n.295-147dup
XM_011542238.1:c.295-147dup	XP_011540540.1:n.295-147dup
XR_946774.1:n.475-147dup
XR_946775.1:n.475-147dup
NM_031475.3:c.295-147dup MANE Select	NP_113663.2:n.295-147dup
XM_011542238.3:c.295-147dup	XP_011540540.1:n.295-147dup
XM_017002433.1:c.295-147dup	XP_016857922.1:n.295-147dup
XM_017002434.1:c.295-147dup	XP_016857923.1:n.295-147dup
XM_024450116.1:c.295-147dup	XP_024305884.1:n.295-147dup
NM_001367473.1:c.295-147dup	NP_001354402.1:n.295-147dup
NM_001367474.1:c.295-147dup	NP_001354403.1:n.295-147dup