Canonical Allele Identifier: CA636016528

Gene: EPPIN EPPIN-WFDC6

Linked Data

• dbSNP Id: rs1211430867
• gnomAD v2: 20-44175997-G-A
• MyVariant Identifiers: chr20:g.44175997G>A (hg19) ; chr20:g.45547358G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45547358G>A , CM000682.2:g.45547358G>A	GRCh38
NC_000020.10:g.44175997G>A , CM000682.1:g.44175997G>A	GRCh37
NC_000020.9:g.43609411G>A	NCBI36

Transcript Alleles

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