Canonical Allele Identifier: CA16024217

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112157610C>A (hg19) ; chr5:g.112821913C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821913C>A , CM000667.2:g.112821913C>A	GRCh38
NC_000005.9:g.112157610C>A , CM000667.1:g.112157610C>A	GRCh37
NC_000005.8:g.112185509C>A	NCBI36
NG_008481.4:g.134393C>A , LRG_130:g.134393C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1330C>A	ENSP00000484935.2:p.His444Asn
ENST00000504915.3:c.1330C>A	ENSP00000473355.2:p.His444Asn
ENST00000505084.2:n.1386C>A
ENST00000505350.2:c.*1336C>A	ENSP00000481752.1:n.*1336C>A
ENST00000507379.6:c.1276C>A	ENSP00000423224.2:p.His426Asn
ENST00000509732.6:c.1330C>A	ENSP00000426541.2:p.His444Asn
ENST00000512211.7:c.1330C>A	ENSP00000423828.3:p.His444Asn
ENST00000257430.9:c.1330C>A MANE Select	ENSP00000257430.4:p.His444Asn
ENST00000257430.8:c.1330C>A	ENSP00000257430.4:p.His444Asn
ENST00000502371.2:c.18C>A
ENST00000507379.5:c.1276C>A	ENSP00000423224.1:p.His426Asn
ENST00000508376.6:c.1330C>A	ENSP00000427089.2:p.His444Asn
ENST00000508624.5:c.*652C>A	ENSP00000424265.1:n.*652C>A
ENST00000512211.6:c.1330C>A	ENSP00000423828.2:p.His444Asn
NM_000038.5:c.1330C>A	NP_000029.2:p.His444Asn
NM_001127510.2:c.1330C>A	NP_001120982.1:p.His444Asn
NM_001127511.2:c.1276C>A	NP_001120983.2:p.His426Asn
NM_001354895.1:c.1330C>A	NP_001341824.1:p.His444Asn
NM_001354896.1:c.1330C>A	NP_001341825.1:p.His444Asn
NM_001354897.1:c.1360C>A	NP_001341826.1:p.His454Asn
NM_001354898.1:c.1255C>A	NP_001341827.1:p.His419Asn
NM_001354899.1:c.1246C>A	NP_001341828.1:p.His416Asn
NM_001354900.1:c.1153C>A	NP_001341829.1:p.His385Asn
NM_001354901.1:c.1153C>A	NP_001341830.1:p.His385Asn
NM_001354902.1:c.1057C>A	NP_001341831.1:p.His353Asn
NM_001354903.1:c.1027C>A	NP_001341832.1:p.His343Asn
NM_001354904.1:c.952C>A	NP_001341833.1:p.His318Asn
NM_001354905.1:c.850C>A	NP_001341834.1:p.His284Asn
NM_001354906.1:c.481C>A	NP_001341835.1:p.His161Asn
NM_000038.6:c.1330C>A MANE Select	NP_000029.2:p.His444Asn
NM_001127510.3:c.1330C>A	NP_001120982.1:p.His444Asn
NM_001127511.3:c.1276C>A	NP_001120983.2:p.His426Asn
NM_001354895.2:c.1330C>A	NP_001341824.1:p.His444Asn
NM_001354896.2:c.1330C>A	NP_001341825.1:p.His444Asn
NM_001354897.2:c.1360C>A	NP_001341826.1:p.His454Asn
NM_001354898.2:c.1255C>A	NP_001341827.1:p.His419Asn
NM_001354899.2:c.1246C>A	NP_001341828.1:p.His416Asn
NM_001354900.2:c.1153C>A	NP_001341829.1:p.His385Asn
NM_001354901.2:c.1153C>A	NP_001341830.1:p.His385Asn
NM_001354902.2:c.1057C>A	NP_001341831.1:p.His353Asn
NM_001354903.2:c.1027C>A	NP_001341832.1:p.His343Asn
NM_001354904.2:c.952C>A	NP_001341833.1:p.His318Asn
NM_001354905.2:c.850C>A	NP_001341834.1:p.His284Asn
NM_001354906.2:c.481C>A	NP_001341835.1:p.His161Asn