Canonical Allele Identifier: CA9878943

Gene: EPPIN EPPIN-WFDC6

Linked Data

• dbSNP Id: rs779612419
• ExAC: 20:44176028 C / T
• gnomAD v2: 20-44176028-C-T
• gnomAD v4: 20-45547389-C-T
• MyVariant Identifiers: chr20:g.44176028C>T (hg19) ; chr20:g.45547389C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45547389C>T , CM000682.2:g.45547389C>T	GRCh38
NC_000020.10:g.44176028C>T , CM000682.1:g.44176028C>T	GRCh37
NC_000020.9:g.43609442C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354280.9:c.-32G>A (EPPIN) MANE Select	ENSP00000361746.4:n.-32G>A
ENST00000651288.1:c.-32G>A (EPPIN-WFDC6)	ENSP00000498632.1:n.-32G>A
ENST00000354280.8:c.-32G>A (EPPIN)	ENSP00000361746.3:n.-32G>A
ENST00000409554.1:c.-32G>A (EPPIN)	ENSP00000387153.1:n.-32G>A
ENST00000504988.1:c.-32G>A (EPPIN-WFDC6)	ENSP00000424176.1:n.-32G>A
NM_001198986.1:c.-32G>A (EPPIN-WFDC6)	NP_001185915.1:n.-32G>A
NM_001302861.1:c.-32G>A (EPPIN)	NP_001289790.1:n.-32G>A
NM_020398.3:c.-32G>A (EPPIN)	NP_065131.1:n.-32G>A
NM_001198986.2:c.-32G>A (EPPIN-WFDC6)	NP_001185915.1:n.-32G>A
NM_001302861.2:c.-32G>A (EPPIN)	NP_001289790.1:n.-32G>A
NM_020398.4:c.-32G>A (EPPIN) MANE Select	NP_065131.1:n.-32G>A