Canonical Allele Identifier: CA8891018
Gene: APCDD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10471735G>A , CM000680.2:g.10471735G>A GRCh38
NC_000018.9:g.10471732G>A , CM000680.1:g.10471732G>A GRCh37
NC_000018.8:g.10461732G>A NCBI36
NG_027685.1:g.22108G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355285.10:c.448G>A MANE Select ENSP00000347433.4:p.Val150Ile
ENST00000355285.9:c.448G>A ENSP00000347433.4:p.Val150Ile
ENST00000423585.2:c.59-13727G>A ENSP00000404930.2:n.59-13727G>A
ENST00000578882.1:c.448G>A ENSP00000463104.1:p.Val150Ile
ENST00000582723.1:c.*195G>A ENSP00000463110.1:n.*195G>A
NM_153000.4:c.448G>A NP_694545.1:p.Val150Ile
XM_011525603.1:c.448G>A XP_011523905.1:p.Val150Ile
XM_011525603.2:c.448G>A XP_011523905.1:p.Val150Ile
NM_153000.5:c.448G>A MANE Select NP_694545.1:p.Val150Ile