Canonical Allele Identifier: CA838218526

Gene: EPDR1 SFRP4

Linked Data

• dbSNP Id: rs1464774863
• gnomAD v3: 7-37949480-T-C
• gnomAD v4: 7-37949480-T-C
• MyVariant Identifiers: chr7:g.37989082T>C (hg19) ; chr7:g.37949480T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37949480T>C , CM000669.2:g.37949480T>C	GRCh38
NC_000007.13:g.37989082T>C , CM000669.1:g.37989082T>C	GRCh37
NC_000007.12:g.37955607T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000199448.9:c.478+432T>C (EPDR1) MANE Select	ENSP00000199448.4:n.478+432T>C
ENST00000199448.8:c.478+432T>C (EPDR1)	ENSP00000199448.4:n.478+432T>C
ENST00000423717.1:c.270-720T>C (EPDR1)	ENSP00000409211.1:n.270-720T>C
ENST00000425345.1:c.295+432T>C (EPDR1)	ENSP00000413359.1:n.295+432T>C
ENST00000447200.2:c.-52-22706A>G (SFRP4)	ENSP00000402262.2:n.-52-22706A>G
ENST00000476620.1:c.172+432T>C (EPDR1)	ENSP00000425858.1:n.172+432T>C
NM_001242946.1:c.270-720T>C (EPDR1)	NP_001229875.2:n.270-720T>C
NM_001242948.1:c.295+432T>C (EPDR1)	NP_001229877.1:n.295+432T>C
NM_017549.4:c.478+432T>C (EPDR1)	NP_060019.2:n.478+432T>C
NM_017549.5:c.478+432T>C (EPDR1) MANE Select	NP_060019.2:n.478+432T>C
NM_001242946.2:c.270-720T>C (EPDR1)	NP_001229875.2:n.270-720T>C
NM_001242948.2:c.295+432T>C (EPDR1)	NP_001229877.1:n.295+432T>C