Canonical Allele Identifier: CA409177709

Gene: EPPIN EPPIN-WFDC6

Linked Data

• MyVariant Identifiers: chr20:g.44175956A>G (hg19) ; chr20:g.45547317A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45547317A>G , CM000682.2:g.45547317A>G	GRCh38
NC_000020.10:g.44175956A>G , CM000682.1:g.44175956A>G	GRCh37
NC_000020.9:g.43609370A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354280.9:c.41T>C (EPPIN) MANE Select	ENSP00000361746.4:p.Val14Ala
ENST00000651288.1:c.41T>C (EPPIN-WFDC6)	ENSP00000498632.1:p.Val14Ala
ENST00000354280.8:c.41T>C (EPPIN)	ENSP00000361746.3:p.Val14Ala
ENST00000409554.1:c.41T>C (EPPIN)	ENSP00000387153.1:p.Val14Ala
ENST00000496898.1:n.41T>C (EPPIN)
ENST00000504988.1:c.41T>C (EPPIN-WFDC6)	ENSP00000424176.1:p.Val14Ala
NM_001198986.1:c.41T>C (EPPIN-WFDC6)	NP_001185915.1:p.Val14Ala
NM_001302861.1:c.41T>C (EPPIN)	NP_001289790.1:p.Val14Ala
NM_020398.3:c.41T>C (EPPIN)	NP_065131.1:p.Val14Ala
NM_001198986.2:c.41T>C (EPPIN-WFDC6)	NP_001185915.1:p.Val14Ala
NM_001302861.2:c.41T>C (EPPIN)	NP_001289790.1:p.Val14Ala
NM_020398.4:c.41T>C (EPPIN) MANE Select	NP_065131.1:p.Val14Ala