Canonical Allele Identifier: CA574229184

Gene: EPDR1 SFRP4

Linked Data

• dbSNP Id: rs1344916777
• gnomAD v2: 7-37988653-A-C
• gnomAD v3: 7-37949051-A-C
• gnomAD v4: 7-37949051-A-C
• MyVariant Identifiers: chr7:g.37988653A>C (hg19) ; chr7:g.37949051A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37949051A>C , CM000669.2:g.37949051A>C	GRCh38
NC_000007.13:g.37988653A>C , CM000669.1:g.37988653A>C	GRCh37
NC_000007.12:g.37955178A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000199448.9:c.478+3A>C (EPDR1) MANE Select	ENSP00000199448.4:n.478+3A>C
ENST00000199448.8:c.478+3A>C (EPDR1)	ENSP00000199448.4:n.478+3A>C
ENST00000423717.1:c.270-1149A>C (EPDR1)	ENSP00000409211.1:n.270-1149A>C
ENST00000425345.1:c.295+3A>C (EPDR1)	ENSP00000413359.1:n.295+3A>C
ENST00000447200.2:c.-52-22277T>G (SFRP4)	ENSP00000402262.2:n.-52-22277T>G
ENST00000476620.1:c.172+3A>C (EPDR1)	ENSP00000425858.1:n.172+3A>C
NM_001242946.1:c.270-1149A>C (EPDR1)	NP_001229875.2:n.270-1149A>C
NM_001242948.1:c.295+3A>C (EPDR1)	NP_001229877.1:n.295+3A>C
NM_017549.4:c.478+3A>C (EPDR1)	NP_060019.2:n.478+3A>C
NM_017549.5:c.478+3A>C (EPDR1) MANE Select	NP_060019.2:n.478+3A>C
NM_001242946.2:c.270-1149A>C (EPDR1)	NP_001229875.2:n.270-1149A>C
NM_001242948.2:c.295+3A>C (EPDR1)	NP_001229877.1:n.295+3A>C