Canonical Allele Identifier: CA838218508

Gene: EPDR1 SFRP4

Linked Data

• dbSNP Id: rs1367476061
• gnomAD v3: 7-37949449-G-T
• gnomAD v4: 7-37949449-G-T
• MyVariant Identifiers: chr7:g.37989051G>T (hg19) ; chr7:g.37949449G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37949449G>T , CM000669.2:g.37949449G>T	GRCh38
NC_000007.13:g.37989051G>T , CM000669.1:g.37989051G>T	GRCh37
NC_000007.12:g.37955576G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000199448.9:c.478+401G>T (EPDR1) MANE Select	ENSP00000199448.4:n.478+401G>T
ENST00000199448.8:c.478+401G>T (EPDR1)	ENSP00000199448.4:n.478+401G>T
ENST00000423717.1:c.270-751G>T (EPDR1)	ENSP00000409211.1:n.270-751G>T
ENST00000425345.1:c.295+401G>T (EPDR1)	ENSP00000413359.1:n.295+401G>T
ENST00000447200.2:c.-52-22675C>A (SFRP4)	ENSP00000402262.2:n.-52-22675C>A
ENST00000476620.1:c.172+401G>T (EPDR1)	ENSP00000425858.1:n.172+401G>T
NM_001242946.1:c.270-751G>T (EPDR1)	NP_001229875.2:n.270-751G>T
NM_001242948.1:c.295+401G>T (EPDR1)	NP_001229877.1:n.295+401G>T
NM_017549.4:c.478+401G>T (EPDR1)	NP_060019.2:n.478+401G>T
NM_017549.5:c.478+401G>T (EPDR1) MANE Select	NP_060019.2:n.478+401G>T
NM_001242946.2:c.270-751G>T (EPDR1)	NP_001229875.2:n.270-751G>T
NM_001242948.2:c.295+401G>T (EPDR1)	NP_001229877.1:n.295+401G>T