Canonical Allele Identifier: CA8891091
Gene: APCDD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10472041C>G , CM000680.2:g.10472041C>G GRCh38
NC_000018.9:g.10472038C>G , CM000680.1:g.10472038C>G GRCh37
NC_000018.8:g.10462038C>G NCBI36
NG_027685.1:g.22414C>G

Transcript Alleles

HGVS Amino-acid Change
NM_153000.5:c.754C>G MANE Select NP_694545.1:p.Pro252Ala
ENST00000355285.10:c.754C>G MANE Select ENSP00000347433.4:p.Pro252Ala
NM_153000.4:c.754C>G NP_694545.1:p.Pro252Ala
ENST00000355285.9:c.754C>G ENSP00000347433.4:p.Pro252Ala
ENST00000423585.2:c.59-13421C>G ENSP00000404930.2:n.59-13421C>G
ENST00000578882.1:c.453+301C>G ENSP00000463104.1:n.453+301C>G
ENST00000579685.1:c.35C>G ENSP00000464649.1:p.Ala12Gly
ENST00000582723.1:c.*501C>G ENSP00000463110.1:n.*501C>G
ENST00000584596.2:c.206C>G
XM_011525603.1:c.754C>G XP_011523905.1:p.Pro252Ala
XM_011525603.2:c.754C>G XP_011523905.1:p.Pro252Ala