Canonical Allele Identifier: CA16033949

Gene: APC

Linked Data

• dbSNP Id: rs2149948664
• MyVariant Identifiers: chr5:g.112177058C>A (hg19) ; chr5:g.112841361C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841361C>A , CM000667.2:g.112841361C>A	GRCh38
NC_000005.9:g.112177058C>A , CM000667.1:g.112177058C>A	GRCh37
NC_000005.8:g.112204957C>A	NCBI36
NG_008481.4:g.153841C>A , LRG_130:g.153841C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5821C>A	ENSP00000473355.2:p.Pro1941Thr
ENST00000505350.2:c.*5773C>A	ENSP00000481752.1:n.*5773C>A
ENST00000507379.6:c.5713C>A	ENSP00000423224.2:p.Pro1905Thr
ENST00000509732.6:c.5767C>A	ENSP00000426541.2:p.Pro1923Thr
ENST00000512211.7:c.5767C>A	ENSP00000423828.3:p.Pro1923Thr
ENST00000257430.9:c.5767C>A MANE Select	ENSP00000257430.4:p.Pro1923Thr
ENST00000257430.8:c.5767C>A	ENSP00000257430.4:p.Pro1923Thr
ENST00000508376.6:c.5767C>A	ENSP00000427089.2:p.Pro1923Thr
ENST00000508624.5:c.*5089C>A	ENSP00000424265.1:n.*5089C>A
ENST00000520401.1:c.230+12389C>A
NM_000038.5:c.5767C>A	NP_000029.2:p.Pro1923Thr
NM_001127510.2:c.5767C>A	NP_001120982.1:p.Pro1923Thr
NM_001127511.2:c.5713C>A	NP_001120983.2:p.Pro1905Thr
NM_001354895.1:c.5767C>A	NP_001341824.1:p.Pro1923Thr
NM_001354896.1:c.5821C>A	NP_001341825.1:p.Pro1941Thr
NM_001354897.1:c.5797C>A	NP_001341826.1:p.Pro1933Thr
NM_001354898.1:c.5692C>A	NP_001341827.1:p.Pro1898Thr
NM_001354899.1:c.5683C>A	NP_001341828.1:p.Pro1895Thr
NM_001354900.1:c.5644C>A	NP_001341829.1:p.Pro1882Thr
NM_001354901.1:c.5590C>A	NP_001341830.1:p.Pro1864Thr
NM_001354902.1:c.5494C>A	NP_001341831.1:p.Pro1832Thr
NM_001354903.1:c.5464C>A	NP_001341832.1:p.Pro1822Thr
NM_001354904.1:c.5389C>A	NP_001341833.1:p.Pro1797Thr
NM_001354905.1:c.5287C>A	NP_001341834.1:p.Pro1763Thr
NM_001354906.1:c.4918C>A	NP_001341835.1:p.Pro1640Thr
NM_000038.6:c.5767C>A MANE Select	NP_000029.2:p.Pro1923Thr
NM_001127510.3:c.5767C>A	NP_001120982.1:p.Pro1923Thr
NM_001127511.3:c.5713C>A	NP_001120983.2:p.Pro1905Thr
NM_001354895.2:c.5767C>A	NP_001341824.1:p.Pro1923Thr
NM_001354896.2:c.5821C>A	NP_001341825.1:p.Pro1941Thr
NM_001354897.2:c.5797C>A	NP_001341826.1:p.Pro1933Thr
NM_001354898.2:c.5692C>A	NP_001341827.1:p.Pro1898Thr
NM_001354899.2:c.5683C>A	NP_001341828.1:p.Pro1895Thr
NM_001354900.2:c.5644C>A	NP_001341829.1:p.Pro1882Thr
NM_001354901.2:c.5590C>A	NP_001341830.1:p.Pro1864Thr
NM_001354902.2:c.5494C>A	NP_001341831.1:p.Pro1832Thr
NM_001354903.2:c.5464C>A	NP_001341832.1:p.Pro1822Thr
NM_001354904.2:c.5389C>A	NP_001341833.1:p.Pro1797Thr
NM_001354905.2:c.5287C>A	NP_001341834.1:p.Pro1763Thr
NM_001354906.2:c.4918C>A	NP_001341835.1:p.Pro1640Thr