Canonical Allele Identifier: CA16031872

Gene: APC

Linked Data

• dbSNP Id: rs1017844073
• MyVariant Identifiers: chr5:g.112176101C>G (hg19) ; chr5:g.112840404C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840404C>G , CM000667.2:g.112840404C>G	GRCh38
NC_000005.9:g.112176101C>G , CM000667.1:g.112176101C>G	GRCh37
NC_000005.8:g.112204000C>G	NCBI36
NG_008481.4:g.152884C>G , LRG_130:g.152884C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4864C>G	ENSP00000473355.2:p.Pro1622Ala
ENST00000505350.2:c.*4816C>G	ENSP00000481752.1:n.*4816C>G
ENST00000507379.6:c.4756C>G	ENSP00000423224.2:p.Pro1586Ala
ENST00000509732.6:c.4810C>G	ENSP00000426541.2:p.Pro1604Ala
ENST00000512211.7:c.4810C>G	ENSP00000423828.3:p.Pro1604Ala
ENST00000257430.9:c.4810C>G MANE Select	ENSP00000257430.4:p.Pro1604Ala
ENST00000257430.8:c.4810C>G	ENSP00000257430.4:p.Pro1604Ala
ENST00000508376.6:c.4810C>G	ENSP00000427089.2:p.Pro1604Ala
ENST00000508624.5:c.*4132C>G	ENSP00000424265.1:n.*4132C>G
ENST00000520401.1:c.230+11432C>G
NM_000038.5:c.4810C>G	NP_000029.2:p.Pro1604Ala
NM_001127510.2:c.4810C>G	NP_001120982.1:p.Pro1604Ala
NM_001127511.2:c.4756C>G	NP_001120983.2:p.Pro1586Ala
NM_001354895.1:c.4810C>G	NP_001341824.1:p.Pro1604Ala
NM_001354896.1:c.4864C>G	NP_001341825.1:p.Pro1622Ala
NM_001354897.1:c.4840C>G	NP_001341826.1:p.Pro1614Ala
NM_001354898.1:c.4735C>G	NP_001341827.1:p.Pro1579Ala
NM_001354899.1:c.4726C>G	NP_001341828.1:p.Pro1576Ala
NM_001354900.1:c.4687C>G	NP_001341829.1:p.Pro1563Ala
NM_001354901.1:c.4633C>G	NP_001341830.1:p.Pro1545Ala
NM_001354902.1:c.4537C>G	NP_001341831.1:p.Pro1513Ala
NM_001354903.1:c.4507C>G	NP_001341832.1:p.Pro1503Ala
NM_001354904.1:c.4432C>G	NP_001341833.1:p.Pro1478Ala
NM_001354905.1:c.4330C>G	NP_001341834.1:p.Pro1444Ala
NM_001354906.1:c.3961C>G	NP_001341835.1:p.Pro1321Ala
NM_000038.6:c.4810C>G MANE Select	NP_000029.2:p.Pro1604Ala
NM_001127510.3:c.4810C>G	NP_001120982.1:p.Pro1604Ala
NM_001127511.3:c.4756C>G	NP_001120983.2:p.Pro1586Ala
NM_001354895.2:c.4810C>G	NP_001341824.1:p.Pro1604Ala
NM_001354896.2:c.4864C>G	NP_001341825.1:p.Pro1622Ala
NM_001354897.2:c.4840C>G	NP_001341826.1:p.Pro1614Ala
NM_001354898.2:c.4735C>G	NP_001341827.1:p.Pro1579Ala
NM_001354899.2:c.4726C>G	NP_001341828.1:p.Pro1576Ala
NM_001354900.2:c.4687C>G	NP_001341829.1:p.Pro1563Ala
NM_001354901.2:c.4633C>G	NP_001341830.1:p.Pro1545Ala
NM_001354902.2:c.4537C>G	NP_001341831.1:p.Pro1513Ala
NM_001354903.2:c.4507C>G	NP_001341832.1:p.Pro1503Ala
NM_001354904.2:c.4432C>G	NP_001341833.1:p.Pro1478Ala
NM_001354905.2:c.4330C>G	NP_001341834.1:p.Pro1444Ala
NM_001354906.2:c.3961C>G	NP_001341835.1:p.Pro1321Ala