Canonical Allele Identifier: CA9044786
Gene: APC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1455391C>T , CM000681.2:g.1455391C>T GRCh38
NC_000019.9:g.1455390C>T , CM000681.1:g.1455390C>T GRCh37
NC_000019.8:g.1406390C>T NCBI36
NG_055243.1:g.14124C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005883.3:c.530C>T MANE Select NP_005874.1:p.Ser177Leu
ENST00000590469.6:c.530C>T MANE Select ENSP00000467073.2:p.Ser177Leu
NM_001351273.1:c.527C>T NP_001338202.1:p.Ser176Leu
NM_005883.2:c.530C>T NP_005874.1:p.Ser177Leu
ENST00000233607.6:c.530C>T ENSP00000233607.2:p.Ser177Leu
ENST00000238483.5:c.527C>T ENSP00000238483.5:p.Ser176Leu
ENST00000535453.5:c.530C>T ENSP00000442954.1:p.Ser177Leu
ENST00000590469.5:c.530C>T ENSP00000467073.1:p.Ser177Leu
ENST00000590877.5:c.527C>T ENSP00000466173.2:p.Ser176Leu
ENST00000593146.1:n.589C>T
XM_005259475.2:c.602C>T XP_005259532.1:p.Ser201Leu
XM_006722607.2:c.599C>T XP_006722670.1:p.Ser200Leu
XM_006722608.2:c.530C>T XP_006722671.1:p.Ser177Leu
XM_006722608.3:c.833C>T XP_006722671.2:p.Ser278Leu
XM_006722609.2:c.530C>T XP_006722672.1:p.Ser177Leu
XM_006722609.3:c.530C>T XP_006722672.1:p.Ser177Leu
XM_006722610.2:c.527C>T XP_006722673.1:p.Ser176Leu
XM_006722610.3:c.830C>T XP_006722673.2:p.Ser277Leu