Canonical Allele Identifier: CA007770

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838333T>C , CM000667.2:g.112838333T>C	GRCh38
NC_000005.9:g.112174030T>C , CM000667.1:g.112174030T>C	GRCh37
NC_000005.8:g.112201929T>C	NCBI36
NG_008481.4:g.150813T>C , LRG_130:g.150813T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2404T>C	ENSP00000484935.2:n.2404T>C
ENST00000504915.3:c.2793T>C	ENSP00000473355.2:p.His931=
ENST00000505350.2:c.*2745T>C	ENSP00000481752.1:n.*2745T>C
ENST00000507379.6:c.2685T>C	ENSP00000423224.2:p.His895=
ENST00000509732.6:c.2739T>C	ENSP00000426541.2:p.His913=
ENST00000512211.7:c.2739T>C	ENSP00000423828.3:p.His913=
ENST00000257430.9:c.2739T>C MANE Select	ENSP00000257430.4:p.His913=
ENST00000257430.8:c.2739T>C	ENSP00000257430.4:p.His913=
ENST00000502371.2:c.1092T>C
ENST00000507379.5:c.2685T>C	ENSP00000423224.1:p.His895=
ENST00000508376.6:c.2739T>C	ENSP00000427089.2:p.His913=
ENST00000508624.5:c.*2061T>C	ENSP00000424265.1:n.*2061T>C
ENST00000512211.6:c.2739T>C	ENSP00000423828.2:p.His913=
ENST00000520401.1:c.230+9361T>C
NM_000038.5:c.2739T>C	NP_000029.2:p.His913=
NM_001127510.2:c.2739T>C	NP_001120982.1:p.His913=
NM_001127511.2:c.2685T>C	NP_001120983.2:p.His895=
NM_001354895.1:c.2739T>C	NP_001341824.1:p.His913=
NM_001354896.1:c.2793T>C	NP_001341825.1:p.His931=
NM_001354897.1:c.2769T>C	NP_001341826.1:p.His923=
NM_001354898.1:c.2664T>C	NP_001341827.1:p.His888=
NM_001354899.1:c.2655T>C	NP_001341828.1:p.His885=
NM_001354900.1:c.2616T>C	NP_001341829.1:p.His872=
NM_001354901.1:c.2562T>C	NP_001341830.1:p.His854=
NM_001354902.1:c.2466T>C	NP_001341831.1:p.His822=
NM_001354903.1:c.2436T>C	NP_001341832.1:p.His812=
NM_001354904.1:c.2361T>C	NP_001341833.1:p.His787=
NM_001354905.1:c.2259T>C	NP_001341834.1:p.His753=
NM_001354906.1:c.1890T>C	NP_001341835.1:p.His630=
NM_000038.6:c.2739T>C MANE Select	NP_000029.2:p.His913=
NM_001127510.3:c.2739T>C	NP_001120982.1:p.His913=
NM_001127511.3:c.2685T>C	NP_001120983.2:p.His895=
NM_001354895.2:c.2739T>C	NP_001341824.1:p.His913=
NM_001354896.2:c.2793T>C	NP_001341825.1:p.His931=
NM_001354897.2:c.2769T>C	NP_001341826.1:p.His923=
NM_001354898.2:c.2664T>C	NP_001341827.1:p.His888=
NM_001354899.2:c.2655T>C	NP_001341828.1:p.His885=
NM_001354900.2:c.2616T>C	NP_001341829.1:p.His872=
NM_001354901.2:c.2562T>C	NP_001341830.1:p.His854=
NM_001354902.2:c.2466T>C	NP_001341831.1:p.His822=
NM_001354903.2:c.2436T>C	NP_001341832.1:p.His812=
NM_001354904.2:c.2361T>C	NP_001341833.1:p.His787=
NM_001354905.2:c.2259T>C	NP_001341834.1:p.His753=
NM_001354906.2:c.1890T>C	NP_001341835.1:p.His630=