Canonical Allele Identifier: CA367217295

Gene: EPDR1 SFRP4

Linked Data

• MyVariant Identifiers: chr7:g.37988650T>G (hg19) ; chr7:g.37949048T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37949048T>G , CM000669.2:g.37949048T>G	GRCh38
NC_000007.13:g.37988650T>G , CM000669.1:g.37988650T>G	GRCh37
NC_000007.12:g.37955175T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000199448.9:c.478T>G (EPDR1) MANE Select	ENSP00000199448.4:p.Tyr160Asp
ENST00000199448.8:c.478T>G (EPDR1)	ENSP00000199448.4:p.Tyr160Asp
ENST00000423717.1:c.270-1152T>G (EPDR1)	ENSP00000409211.1:n.270-1152T>G
ENST00000425345.1:c.295T>G (EPDR1)	ENSP00000413359.1:p.Tyr99Asp
ENST00000447200.2:c.-52-22274A>C (SFRP4)	ENSP00000402262.2:n.-52-22274A>C
ENST00000476620.1:c.172T>G (EPDR1)	ENSP00000425858.1:p.Tyr58Asp
NM_001242946.1:c.270-1152T>G (EPDR1)	NP_001229875.2:n.270-1152T>G
NM_001242948.1:c.295T>G (EPDR1)	NP_001229877.1:p.Tyr99Asp
NM_017549.4:c.478T>G (EPDR1)	NP_060019.2:p.Tyr160Asp
NM_017549.5:c.478T>G (EPDR1) MANE Select	NP_060019.2:p.Tyr160Asp
NM_001242946.2:c.270-1152T>G (EPDR1)	NP_001229875.2:n.270-1152T>G
NM_001242948.2:c.295T>G (EPDR1)	NP_001229877.1:p.Tyr99Asp