Canonical Allele Identifier: CA16024535

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112162871A>C (hg19) ; chr5:g.112827174A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827174A>C , CM000667.2:g.112827174A>C	GRCh38
NC_000005.9:g.112162871A>C , CM000667.1:g.112162871A>C	GRCh37
NC_000005.8:g.112190770A>C	NCBI36
NG_008481.4:g.139654A>C , LRG_130:g.139654A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5183A>C	ENSP00000484935.2:n.1408+5183A>C
ENST00000504915.3:c.1529A>C	ENSP00000473355.2:p.His510Pro
ENST00000505084.2:n.1531A>C
ENST00000505350.2:c.*1481A>C	ENSP00000481752.1:n.*1481A>C
ENST00000507379.6:c.1421A>C	ENSP00000423224.2:p.His474Pro
ENST00000509732.6:c.1475A>C	ENSP00000426541.2:p.His492Pro
ENST00000512211.7:c.1475A>C	ENSP00000423828.3:p.His492Pro
ENST00000257430.9:c.1475A>C MANE Select	ENSP00000257430.4:p.His492Pro
ENST00000257430.8:c.1475A>C	ENSP00000257430.4:p.His492Pro
ENST00000502371.2:c.96+5183A>C
ENST00000504915.2:c.164A>C	ENSP00000473355.1:p.His55Pro
ENST00000507379.5:c.1421A>C	ENSP00000423224.1:p.His474Pro
ENST00000508376.6:c.1475A>C	ENSP00000427089.2:p.His492Pro
ENST00000508624.5:c.*797A>C	ENSP00000424265.1:n.*797A>C
ENST00000512211.6:c.1475A>C	ENSP00000423828.2:p.His492Pro
NM_000038.5:c.1475A>C	NP_000029.2:p.His492Pro
NM_001127510.2:c.1475A>C	NP_001120982.1:p.His492Pro
NM_001127511.2:c.1421A>C	NP_001120983.2:p.His474Pro
NM_001354895.1:c.1475A>C	NP_001341824.1:p.His492Pro
NM_001354896.1:c.1529A>C	NP_001341825.1:p.His510Pro
NM_001354897.1:c.1505A>C	NP_001341826.1:p.His502Pro
NM_001354898.1:c.1400A>C	NP_001341827.1:p.His467Pro
NM_001354899.1:c.1391A>C	NP_001341828.1:p.His464Pro
NM_001354900.1:c.1352A>C	NP_001341829.1:p.His451Pro
NM_001354901.1:c.1298A>C	NP_001341830.1:p.His433Pro
NM_001354902.1:c.1202A>C	NP_001341831.1:p.His401Pro
NM_001354903.1:c.1172A>C	NP_001341832.1:p.His391Pro
NM_001354904.1:c.1097A>C	NP_001341833.1:p.His366Pro
NM_001354905.1:c.995A>C	NP_001341834.1:p.His332Pro
NM_001354906.1:c.626A>C	NP_001341835.1:p.His209Pro
NM_000038.6:c.1475A>C MANE Select	NP_000029.2:p.His492Pro
NM_001127510.3:c.1475A>C	NP_001120982.1:p.His492Pro
NM_001127511.3:c.1421A>C	NP_001120983.2:p.His474Pro
NM_001354895.2:c.1475A>C	NP_001341824.1:p.His492Pro
NM_001354896.2:c.1529A>C	NP_001341825.1:p.His510Pro
NM_001354897.2:c.1505A>C	NP_001341826.1:p.His502Pro
NM_001354898.2:c.1400A>C	NP_001341827.1:p.His467Pro
NM_001354899.2:c.1391A>C	NP_001341828.1:p.His464Pro
NM_001354900.2:c.1352A>C	NP_001341829.1:p.His451Pro
NM_001354901.2:c.1298A>C	NP_001341830.1:p.His433Pro
NM_001354902.2:c.1202A>C	NP_001341831.1:p.His401Pro
NM_001354903.2:c.1172A>C	NP_001341832.1:p.His391Pro
NM_001354904.2:c.1097A>C	NP_001341833.1:p.His366Pro
NM_001354905.2:c.995A>C	NP_001341834.1:p.His332Pro
NM_001354906.2:c.626A>C	NP_001341835.1:p.His209Pro