Canonical Allele Identifier: CA446210804

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112178344T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842647T>A , CM000667.2:g.112842647T>A	GRCh38
NC_000005.9:g.112178344T>A , CM000667.1:g.112178344T>A	GRCh37
NC_000005.8:g.112206243T>A	NCBI36
NG_008481.4:g.155127T>A , LRG_130:g.155127T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7107T>A	ENSP00000473355.2:p.Pro2369=
ENST00000505350.2:c.*7059T>A	ENSP00000481752.1:n.*7059T>A
ENST00000507379.6:c.6999T>A	ENSP00000423224.2:p.Pro2333=
ENST00000509732.6:c.7053T>A	ENSP00000426541.2:p.Pro2351=
ENST00000512211.7:c.7053T>A	ENSP00000423828.3:p.Pro2351=
ENST00000257430.9:c.7053T>A MANE Select	ENSP00000257430.4:p.Pro2351=
ENST00000257430.8:c.7053T>A	ENSP00000257430.4:p.Pro2351=
ENST00000508376.6:c.7053T>A	ENSP00000427089.2:p.Pro2351=
ENST00000508624.5:c.*6375T>A	ENSP00000424265.1:n.*6375T>A
ENST00000520401.1:c.230+13675T>A
NM_000038.5:c.7053T>A	NP_000029.2:p.Pro2351=
NM_001127510.2:c.7053T>A	NP_001120982.1:p.Pro2351=
NM_001127511.2:c.6999T>A	NP_001120983.2:p.Pro2333=
NM_001354895.1:c.7053T>A	NP_001341824.1:p.Pro2351=
NM_001354896.1:c.7107T>A	NP_001341825.1:p.Pro2369=
NM_001354897.1:c.7083T>A	NP_001341826.1:p.Pro2361=
NM_001354898.1:c.6978T>A	NP_001341827.1:p.Pro2326=
NM_001354899.1:c.6969T>A	NP_001341828.1:p.Pro2323=
NM_001354900.1:c.6930T>A	NP_001341829.1:p.Pro2310=
NM_001354901.1:c.6876T>A	NP_001341830.1:p.Pro2292=
NM_001354902.1:c.6780T>A	NP_001341831.1:p.Pro2260=
NM_001354903.1:c.6750T>A	NP_001341832.1:p.Pro2250=
NM_001354904.1:c.6675T>A	NP_001341833.1:p.Pro2225=
NM_001354905.1:c.6573T>A	NP_001341834.1:p.Pro2191=
NM_001354906.1:c.6204T>A	NP_001341835.1:p.Pro2068=
NM_000038.6:c.7053T>A MANE Select	NP_000029.2:p.Pro2351=
NM_001127510.3:c.7053T>A	NP_001120982.1:p.Pro2351=
NM_001127511.3:c.6999T>A	NP_001120983.2:p.Pro2333=
NM_001354895.2:c.7053T>A	NP_001341824.1:p.Pro2351=
NM_001354896.2:c.7107T>A	NP_001341825.1:p.Pro2369=
NM_001354897.2:c.7083T>A	NP_001341826.1:p.Pro2361=
NM_001354898.2:c.6978T>A	NP_001341827.1:p.Pro2326=
NM_001354899.2:c.6969T>A	NP_001341828.1:p.Pro2323=
NM_001354900.2:c.6930T>A	NP_001341829.1:p.Pro2310=
NM_001354901.2:c.6876T>A	NP_001341830.1:p.Pro2292=
NM_001354902.2:c.6780T>A	NP_001341831.1:p.Pro2260=
NM_001354903.2:c.6750T>A	NP_001341832.1:p.Pro2250=
NM_001354904.2:c.6675T>A	NP_001341833.1:p.Pro2225=
NM_001354905.2:c.6573T>A	NP_001341834.1:p.Pro2191=
NM_001354906.2:c.6204T>A	NP_001341835.1:p.Pro2068=