Canonical Allele Identifier: CA013705

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843066T>C , CM000667.2:g.112843066T>C	GRCh38
NC_000005.9:g.112178763T>C , CM000667.1:g.112178763T>C	GRCh37
NC_000005.8:g.112206662T>C	NCBI36
NG_008481.4:g.155546T>C , LRG_130:g.155546T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.7472T>C MANE Select	NP_000029.2:p.Met2491Thr
ENST00000257430.9:c.7472T>C MANE Select	ENSP00000257430.4:p.Met2491Thr
NM_000038.5:c.7472T>C	NP_000029.2:p.Met2491Thr
NM_001127510.2:c.7472T>C	NP_001120982.1:p.Met2491Thr
NM_001127510.3:c.7472T>C	NP_001120982.1:p.Met2491Thr
NM_001127511.2:c.7418T>C	NP_001120983.2:p.Met2473Thr
NM_001127511.3:c.7418T>C	NP_001120983.2:p.Met2473Thr
NM_001354895.1:c.7472T>C	NP_001341824.1:p.Met2491Thr
NM_001354895.2:c.7472T>C	NP_001341824.1:p.Met2491Thr
NM_001354896.1:c.7526T>C	NP_001341825.1:p.Met2509Thr
NM_001354896.2:c.7526T>C	NP_001341825.1:p.Met2509Thr
NM_001354897.1:c.7502T>C	NP_001341826.1:p.Met2501Thr
NM_001354897.2:c.7502T>C	NP_001341826.1:p.Met2501Thr
NM_001354898.1:c.7397T>C	NP_001341827.1:p.Met2466Thr
NM_001354898.2:c.7397T>C	NP_001341827.1:p.Met2466Thr
NM_001354899.1:c.7388T>C	NP_001341828.1:p.Met2463Thr
NM_001354899.2:c.7388T>C	NP_001341828.1:p.Met2463Thr
NM_001354900.1:c.7349T>C	NP_001341829.1:p.Met2450Thr
NM_001354900.2:c.7349T>C	NP_001341829.1:p.Met2450Thr
NM_001354901.1:c.7295T>C	NP_001341830.1:p.Met2432Thr
NM_001354901.2:c.7295T>C	NP_001341830.1:p.Met2432Thr
NM_001354902.1:c.7199T>C	NP_001341831.1:p.Met2400Thr
NM_001354902.2:c.7199T>C	NP_001341831.1:p.Met2400Thr
NM_001354903.1:c.7169T>C	NP_001341832.1:p.Met2390Thr
NM_001354903.2:c.7169T>C	NP_001341832.1:p.Met2390Thr
NM_001354904.1:c.7094T>C	NP_001341833.1:p.Met2365Thr
NM_001354904.2:c.7094T>C	NP_001341833.1:p.Met2365Thr
NM_001354905.1:c.6992T>C	NP_001341834.1:p.Met2331Thr
NM_001354905.2:c.6992T>C	NP_001341834.1:p.Met2331Thr
NM_001354906.1:c.6623T>C	NP_001341835.1:p.Met2208Thr
NM_001354906.2:c.6623T>C	NP_001341835.1:p.Met2208Thr
ENST00000257430.8:c.7472T>C	ENSP00000257430.4:p.Met2491Thr
ENST00000504915.3:c.7526T>C	ENSP00000473355.2:p.Met2509Thr
ENST00000505350.2:c.*7478T>C	ENSP00000481752.1:n.*7478T>C
ENST00000507379.6:c.7418T>C	ENSP00000423224.2:p.Met2473Thr
ENST00000508376.6:c.7472T>C	ENSP00000427089.2:p.Met2491Thr
ENST00000509732.6:c.7472T>C	ENSP00000426541.2:p.Met2491Thr
ENST00000512211.7:c.7472T>C	ENSP00000423828.3:p.Met2491Thr
ENST00000520401.1:c.231-13583T>C