Canonical Allele Identifier: CA16028807

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174701A>C (hg19) ; chr5:g.112839004A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839004A>C , CM000667.2:g.112839004A>C	GRCh38
NC_000005.9:g.112174701A>C , CM000667.1:g.112174701A>C	GRCh37
NC_000005.8:g.112202600A>C	NCBI36
NG_008481.4:g.151484A>C , LRG_130:g.151484A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3075A>C	ENSP00000484935.2:n.3075A>C
ENST00000504915.3:c.3464A>C	ENSP00000473355.2:p.Asp1155Ala
ENST00000505350.2:c.*3416A>C	ENSP00000481752.1:n.*3416A>C
ENST00000507379.6:c.3356A>C	ENSP00000423224.2:p.Asp1119Ala
ENST00000509732.6:c.3410A>C	ENSP00000426541.2:p.Asp1137Ala
ENST00000512211.7:c.3410A>C	ENSP00000423828.3:p.Asp1137Ala
ENST00000257430.9:c.3410A>C MANE Select	ENSP00000257430.4:p.Asp1137Ala
ENST00000257430.8:c.3410A>C	ENSP00000257430.4:p.Asp1137Ala
ENST00000502371.2:c.1763A>C
ENST00000507379.5:c.3356A>C	ENSP00000423224.1:p.Asp1119Ala
ENST00000508376.6:c.3410A>C	ENSP00000427089.2:p.Asp1137Ala
ENST00000508624.5:c.*2732A>C	ENSP00000424265.1:n.*2732A>C
ENST00000512211.6:c.3410A>C	ENSP00000423828.2:p.Asp1137Ala
ENST00000520401.1:c.230+10032A>C
NM_000038.5:c.3410A>C	NP_000029.2:p.Asp1137Ala
NM_001127510.2:c.3410A>C	NP_001120982.1:p.Asp1137Ala
NM_001127511.2:c.3356A>C	NP_001120983.2:p.Asp1119Ala
NM_001354895.1:c.3410A>C	NP_001341824.1:p.Asp1137Ala
NM_001354896.1:c.3464A>C	NP_001341825.1:p.Asp1155Ala
NM_001354897.1:c.3440A>C	NP_001341826.1:p.Asp1147Ala
NM_001354898.1:c.3335A>C	NP_001341827.1:p.Asp1112Ala
NM_001354899.1:c.3326A>C	NP_001341828.1:p.Asp1109Ala
NM_001354900.1:c.3287A>C	NP_001341829.1:p.Asp1096Ala
NM_001354901.1:c.3233A>C	NP_001341830.1:p.Asp1078Ala
NM_001354902.1:c.3137A>C	NP_001341831.1:p.Asp1046Ala
NM_001354903.1:c.3107A>C	NP_001341832.1:p.Asp1036Ala
NM_001354904.1:c.3032A>C	NP_001341833.1:p.Asp1011Ala
NM_001354905.1:c.2930A>C	NP_001341834.1:p.Asp977Ala
NM_001354906.1:c.2561A>C	NP_001341835.1:p.Asp854Ala
NM_000038.6:c.3410A>C MANE Select	NP_000029.2:p.Asp1137Ala
NM_001127510.3:c.3410A>C	NP_001120982.1:p.Asp1137Ala
NM_001127511.3:c.3356A>C	NP_001120983.2:p.Asp1119Ala
NM_001354895.2:c.3410A>C	NP_001341824.1:p.Asp1137Ala
NM_001354896.2:c.3464A>C	NP_001341825.1:p.Asp1155Ala
NM_001354897.2:c.3440A>C	NP_001341826.1:p.Asp1147Ala
NM_001354898.2:c.3335A>C	NP_001341827.1:p.Asp1112Ala
NM_001354899.2:c.3326A>C	NP_001341828.1:p.Asp1109Ala
NM_001354900.2:c.3287A>C	NP_001341829.1:p.Asp1096Ala
NM_001354901.2:c.3233A>C	NP_001341830.1:p.Asp1078Ala
NM_001354902.2:c.3137A>C	NP_001341831.1:p.Asp1046Ala
NM_001354903.2:c.3107A>C	NP_001341832.1:p.Asp1036Ala
NM_001354904.2:c.3032A>C	NP_001341833.1:p.Asp1011Ala
NM_001354905.2:c.2930A>C	NP_001341834.1:p.Asp977Ala
NM_001354906.2:c.2561A>C	NP_001341835.1:p.Asp854Ala