Canonical Allele Identifier: CA445963065
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs1765293802
MyVariant Identifiers: chr5:g.112174207T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112838510T>A , CM000667.2:g.112838510T>A GRCh38
NC_000005.9:g.112174207T>A , CM000667.1:g.112174207T>A GRCh37
NC_000005.8:g.112202106T>A NCBI36
NG_008481.4:g.150990T>A , LRG_130:g.150990T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.2581T>A ENSP00000484935.2:n.2581T>A
ENST00000504915.3:c.2970T>A ENSP00000473355.2:p.Gly990=
ENST00000505350.2:c.*2922T>A ENSP00000481752.1:n.*2922T>A
ENST00000507379.6:c.2862T>A ENSP00000423224.2:p.Gly954=
ENST00000509732.6:c.2916T>A ENSP00000426541.2:p.Gly972=
ENST00000512211.7:c.2916T>A ENSP00000423828.3:p.Gly972=
ENST00000257430.9:c.2916T>A MANE Select ENSP00000257430.4:p.Gly972=
ENST00000257430.8:c.2916T>A ENSP00000257430.4:p.Gly972=
ENST00000502371.2:c.1269T>A
ENST00000507379.5:c.2862T>A ENSP00000423224.1:p.Gly954=
ENST00000508376.6:c.2916T>A ENSP00000427089.2:p.Gly972=
ENST00000508624.5:c.*2238T>A ENSP00000424265.1:n.*2238T>A
ENST00000512211.6:c.2916T>A ENSP00000423828.2:p.Gly972=
ENST00000520401.1:c.230+9538T>A
NM_000038.5:c.2916T>A NP_000029.2:p.Gly972=
NM_001127510.2:c.2916T>A NP_001120982.1:p.Gly972=
NM_001127511.2:c.2862T>A NP_001120983.2:p.Gly954=
NM_001354895.1:c.2916T>A NP_001341824.1:p.Gly972=
NM_001354896.1:c.2970T>A NP_001341825.1:p.Gly990=
NM_001354897.1:c.2946T>A NP_001341826.1:p.Gly982=
NM_001354898.1:c.2841T>A NP_001341827.1:p.Gly947=
NM_001354899.1:c.2832T>A NP_001341828.1:p.Gly944=
NM_001354900.1:c.2793T>A NP_001341829.1:p.Gly931=
NM_001354901.1:c.2739T>A NP_001341830.1:p.Gly913=
NM_001354902.1:c.2643T>A NP_001341831.1:p.Gly881=
NM_001354903.1:c.2613T>A NP_001341832.1:p.Gly871=
NM_001354904.1:c.2538T>A NP_001341833.1:p.Gly846=
NM_001354905.1:c.2436T>A NP_001341834.1:p.Gly812=
NM_001354906.1:c.2067T>A NP_001341835.1:p.Gly689=
NM_000038.6:c.2916T>A MANE Select NP_000029.2:p.Gly972=
NM_001127510.3:c.2916T>A NP_001120982.1:p.Gly972=
NM_001127511.3:c.2862T>A NP_001120983.2:p.Gly954=
NM_001354895.2:c.2916T>A NP_001341824.1:p.Gly972=
NM_001354896.2:c.2970T>A NP_001341825.1:p.Gly990=
NM_001354897.2:c.2946T>A NP_001341826.1:p.Gly982=
NM_001354898.2:c.2841T>A NP_001341827.1:p.Gly947=
NM_001354899.2:c.2832T>A NP_001341828.1:p.Gly944=
NM_001354900.2:c.2793T>A NP_001341829.1:p.Gly931=
NM_001354901.2:c.2739T>A NP_001341830.1:p.Gly913=
NM_001354902.2:c.2643T>A NP_001341831.1:p.Gly881=
NM_001354903.2:c.2613T>A NP_001341832.1:p.Gly871=
NM_001354904.2:c.2538T>A NP_001341833.1:p.Gly846=
NM_001354905.2:c.2436T>A NP_001341834.1:p.Gly812=
NM_001354906.2:c.2067T>A NP_001341835.1:p.Gly689=