Canonical Allele Identifier: CA409177711

Gene: EPPIN EPPIN-WFDC6

Linked Data

• MyVariant Identifiers: chr20:g.44175958G>C (hg19) ; chr20:g.45547319G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45547319G>C , CM000682.2:g.45547319G>C	GRCh38
NC_000020.10:g.44175958G>C , CM000682.1:g.44175958G>C	GRCh37
NC_000020.9:g.43609372G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354280.9:c.39C>G (EPPIN) MANE Select	ENSP00000361746.4:p.Phe13Leu
ENST00000651288.1:c.39C>G (EPPIN-WFDC6)	ENSP00000498632.1:p.Phe13Leu
ENST00000354280.8:c.39C>G (EPPIN)	ENSP00000361746.3:p.Phe13Leu
ENST00000409554.1:c.39C>G (EPPIN)	ENSP00000387153.1:p.Phe13Leu
ENST00000496898.1:n.39C>G (EPPIN)
ENST00000504988.1:c.39C>G (EPPIN-WFDC6)	ENSP00000424176.1:p.Phe13Leu
NM_001198986.1:c.39C>G (EPPIN-WFDC6)	NP_001185915.1:p.Phe13Leu
NM_001302861.1:c.39C>G (EPPIN)	NP_001289790.1:p.Phe13Leu
NM_020398.3:c.39C>G (EPPIN)	NP_065131.1:p.Phe13Leu
NM_001198986.2:c.39C>G (EPPIN-WFDC6)	NP_001185915.1:p.Phe13Leu
NM_001302861.2:c.39C>G (EPPIN)	NP_001289790.1:p.Phe13Leu
NM_020398.4:c.39C>G (EPPIN) MANE Select	NP_065131.1:p.Phe13Leu