Canonical Allele Identifier: CA16033951

Gene: APC

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.5821C>T	ENSP00000473355.2:p.Pro1941Ser
ENST00000505350.2:c.*5773C>T	ENSP00000481752.1:n.*5773C>T
ENST00000507379.6:c.5713C>T	ENSP00000423224.2:p.Pro1905Ser
ENST00000509732.6:c.5767C>T	ENSP00000426541.2:p.Pro1923Ser
ENST00000512211.7:c.5767C>T	ENSP00000423828.3:p.Pro1923Ser
ENST00000257430.9:c.5767C>T MANE Select	ENSP00000257430.4:p.Pro1923Ser
ENST00000257430.8:c.5767C>T	ENSP00000257430.4:p.Pro1923Ser
ENST00000508376.6:c.5767C>T	ENSP00000427089.2:p.Pro1923Ser
ENST00000508624.5:c.*5089C>T	ENSP00000424265.1:n.*5089C>T
ENST00000520401.1:c.230+12389C>T
NM_000038.5:c.5767C>T	NP_000029.2:p.Pro1923Ser
NM_001127510.2:c.5767C>T	NP_001120982.1:p.Pro1923Ser
NM_001127511.2:c.5713C>T	NP_001120983.2:p.Pro1905Ser
NM_001354895.1:c.5767C>T	NP_001341824.1:p.Pro1923Ser
NM_001354896.1:c.5821C>T	NP_001341825.1:p.Pro1941Ser
NM_001354897.1:c.5797C>T	NP_001341826.1:p.Pro1933Ser
NM_001354898.1:c.5692C>T	NP_001341827.1:p.Pro1898Ser
NM_001354899.1:c.5683C>T	NP_001341828.1:p.Pro1895Ser
NM_001354900.1:c.5644C>T	NP_001341829.1:p.Pro1882Ser
NM_001354901.1:c.5590C>T	NP_001341830.1:p.Pro1864Ser
NM_001354902.1:c.5494C>T	NP_001341831.1:p.Pro1832Ser
NM_001354903.1:c.5464C>T	NP_001341832.1:p.Pro1822Ser
NM_001354904.1:c.5389C>T	NP_001341833.1:p.Pro1797Ser
NM_001354905.1:c.5287C>T	NP_001341834.1:p.Pro1763Ser
NM_001354906.1:c.4918C>T	NP_001341835.1:p.Pro1640Ser
NM_000038.6:c.5767C>T MANE Select	NP_000029.2:p.Pro1923Ser
NM_001127510.3:c.5767C>T	NP_001120982.1:p.Pro1923Ser
NM_001127511.3:c.5713C>T	NP_001120983.2:p.Pro1905Ser
NM_001354895.2:c.5767C>T	NP_001341824.1:p.Pro1923Ser
NM_001354896.2:c.5821C>T	NP_001341825.1:p.Pro1941Ser
NM_001354897.2:c.5797C>T	NP_001341826.1:p.Pro1933Ser
NM_001354898.2:c.5692C>T	NP_001341827.1:p.Pro1898Ser
NM_001354899.2:c.5683C>T	NP_001341828.1:p.Pro1895Ser
NM_001354900.2:c.5644C>T	NP_001341829.1:p.Pro1882Ser
NM_001354901.2:c.5590C>T	NP_001341830.1:p.Pro1864Ser
NM_001354902.2:c.5494C>T	NP_001341831.1:p.Pro1832Ser
NM_001354903.2:c.5464C>T	NP_001341832.1:p.Pro1822Ser
NM_001354904.2:c.5389C>T	NP_001341833.1:p.Pro1797Ser
NM_001354905.2:c.5287C>T	NP_001341834.1:p.Pro1763Ser
NM_001354906.2:c.4918C>T	NP_001341835.1:p.Pro1640Ser