Canonical Allele Identifier: CA367217262

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37949033A>C , CM000669.2:g.37949033A>C GRCh38
NC_000007.13:g.37988635A>C , CM000669.1:g.37988635A>C GRCh37
NC_000007.12:g.37955160A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000199448.9:c.463A>C (EPDR1) MANE Select ENSP00000199448.4:p.Lys155Gln
ENST00000199448.8:c.463A>C (EPDR1) ENSP00000199448.4:p.Lys155Gln
ENST00000423717.1:c.270-1167A>C (EPDR1) ENSP00000409211.1:n.270-1167A>C
ENST00000425345.1:c.280A>C (EPDR1) ENSP00000413359.1:p.Lys94Gln
ENST00000447200.2:c.-52-22259T>G (SFRP4) ENSP00000402262.2:n.-52-22259T>G
ENST00000476620.1:c.157A>C (EPDR1) ENSP00000425858.1:p.Lys53Gln
NM_001242946.1:c.270-1167A>C (EPDR1) NP_001229875.2:n.270-1167A>C
NM_001242948.1:c.280A>C (EPDR1) NP_001229877.1:p.Lys94Gln
NM_017549.4:c.463A>C (EPDR1) NP_060019.2:p.Lys155Gln
NM_017549.5:c.463A>C (EPDR1) MANE Select NP_060019.2:p.Lys155Gln
NM_001242946.2:c.270-1167A>C (EPDR1) NP_001229875.2:n.270-1167A>C
NM_001242948.2:c.280A>C (EPDR1) NP_001229877.1:p.Lys94Gln