Canonical Allele Identifier: CA2366263857
Gene: EPPIN HGNC NCBI
EPPIN-WFDC6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45547361G= , CM000682.2:g.45547361G= GRCh38
NC_000020.10:g.44176000G= , CM000682.1:g.44176000G= GRCh37
NC_000020.9:g.43609414G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354280.9:c.-4C= (EPPIN) MANE Select ENSP00000361746.4:n.-4C=
ENST00000651288.1:c.-4C= (EPPIN-WFDC6) ENSP00000498632.1:n.-4C=
ENST00000354280.8:c.-4C= (EPPIN) ENSP00000361746.3:n.-4C=
ENST00000409554.1:c.-4C= (EPPIN) ENSP00000387153.1:n.-4C=
ENST00000504988.1:c.-4C= (EPPIN-WFDC6) ENSP00000424176.1:n.-4C=
NM_001198986.1:c.-4C= (EPPIN-WFDC6) NP_001185915.1:n.-4C=
NM_001302861.1:c.-4C= (EPPIN) NP_001289790.1:n.-4C=
NM_020398.3:c.-4C= (EPPIN) NP_065131.1:n.-4C=
NM_001198986.2:c.-4C= (EPPIN-WFDC6) NP_001185915.1:n.-4C=
NM_001302861.2:c.-4C= (EPPIN) NP_001289790.1:n.-4C=
NM_020398.4:c.-4C= (EPPIN) MANE Select NP_065131.1:n.-4C=
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