Canonical Allele Identifier: CA1700817263

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37949607_37949609delinsGTA , CM000669.2:g.37949607_37949609delinsGTA GRCh38
NC_000007.13:g.37989209_37989211delinsGTA , CM000669.1:g.37989209_37989211delinsGTA GRCh37
NC_000007.12:g.37955734_37955736delinsGTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000199448.9:c.478+559_478+561delinsGTA (EPDR1) MANE Select ENSP00000199448.4:n.478+559_478+561delinsGTA
ENST00000199448.8:c.478+559_478+561delinsGTA (EPDR1) ENSP00000199448.4:n.478+559_478+561delinsGTA
ENST00000423717.1:c.270-593_270-591delinsGTA (EPDR1) ENSP00000409211.1:n.270-593_270-591delinsGTA
ENST00000425345.1:c.295+559_295+561delinsGTA (EPDR1) ENSP00000413359.1:n.295+559_295+561delinsGTA
ENST00000447200.2:c.-52-22835_-52-22833delinsTAC (SFRP4) ENSP00000402262.2:n.-52-22835_-52-22833delinsTAC
ENST00000476620.1:c.172+559_172+561delinsGTA (EPDR1) ENSP00000425858.1:n.172+559_172+561delinsGTA
NM_001242946.1:c.270-593_270-591delinsGTA (EPDR1) NP_001229875.2:n.270-593_270-591delinsGTA
NM_001242948.1:c.295+559_295+561delinsGTA (EPDR1) NP_001229877.1:n.295+559_295+561delinsGTA
NM_017549.4:c.478+559_478+561delinsGTA (EPDR1) NP_060019.2:n.478+559_478+561delinsGTA
NM_017549.5:c.478+559_478+561delinsGTA (EPDR1) MANE Select NP_060019.2:n.478+559_478+561delinsGTA
NM_001242946.2:c.270-593_270-591delinsGTA (EPDR1) NP_001229875.2:n.270-593_270-591delinsGTA
NM_001242948.2:c.295+559_295+561delinsGTA (EPDR1) NP_001229877.1:n.295+559_295+561delinsGTA