Canonical Allele Identifier: CA446210574

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112178251T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842554T>G , CM000667.2:g.112842554T>G	GRCh38
NC_000005.9:g.112178251T>G , CM000667.1:g.112178251T>G	GRCh37
NC_000005.8:g.112206150T>G	NCBI36
NG_008481.4:g.155034T>G , LRG_130:g.155034T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7014T>G	ENSP00000473355.2:p.Pro2338=
ENST00000505350.2:c.*6966T>G	ENSP00000481752.1:n.*6966T>G
ENST00000507379.6:c.6906T>G	ENSP00000423224.2:p.Pro2302=
ENST00000509732.6:c.6960T>G	ENSP00000426541.2:p.Pro2320=
ENST00000512211.7:c.6960T>G	ENSP00000423828.3:p.Pro2320=
ENST00000257430.9:c.6960T>G MANE Select	ENSP00000257430.4:p.Pro2320=
ENST00000257430.8:c.6960T>G	ENSP00000257430.4:p.Pro2320=
ENST00000508376.6:c.6960T>G	ENSP00000427089.2:p.Pro2320=
ENST00000508624.5:c.*6282T>G	ENSP00000424265.1:n.*6282T>G
ENST00000520401.1:c.230+13582T>G
NM_000038.5:c.6960T>G	NP_000029.2:p.Pro2320=
NM_001127510.2:c.6960T>G	NP_001120982.1:p.Pro2320=
NM_001127511.2:c.6906T>G	NP_001120983.2:p.Pro2302=
NM_001354895.1:c.6960T>G	NP_001341824.1:p.Pro2320=
NM_001354896.1:c.7014T>G	NP_001341825.1:p.Pro2338=
NM_001354897.1:c.6990T>G	NP_001341826.1:p.Pro2330=
NM_001354898.1:c.6885T>G	NP_001341827.1:p.Pro2295=
NM_001354899.1:c.6876T>G	NP_001341828.1:p.Pro2292=
NM_001354900.1:c.6837T>G	NP_001341829.1:p.Pro2279=
NM_001354901.1:c.6783T>G	NP_001341830.1:p.Pro2261=
NM_001354902.1:c.6687T>G	NP_001341831.1:p.Pro2229=
NM_001354903.1:c.6657T>G	NP_001341832.1:p.Pro2219=
NM_001354904.1:c.6582T>G	NP_001341833.1:p.Pro2194=
NM_001354905.1:c.6480T>G	NP_001341834.1:p.Pro2160=
NM_001354906.1:c.6111T>G	NP_001341835.1:p.Pro2037=
NM_000038.6:c.6960T>G MANE Select	NP_000029.2:p.Pro2320=
NM_001127510.3:c.6960T>G	NP_001120982.1:p.Pro2320=
NM_001127511.3:c.6906T>G	NP_001120983.2:p.Pro2302=
NM_001354895.2:c.6960T>G	NP_001341824.1:p.Pro2320=
NM_001354896.2:c.7014T>G	NP_001341825.1:p.Pro2338=
NM_001354897.2:c.6990T>G	NP_001341826.1:p.Pro2330=
NM_001354898.2:c.6885T>G	NP_001341827.1:p.Pro2295=
NM_001354899.2:c.6876T>G	NP_001341828.1:p.Pro2292=
NM_001354900.2:c.6837T>G	NP_001341829.1:p.Pro2279=
NM_001354901.2:c.6783T>G	NP_001341830.1:p.Pro2261=
NM_001354902.2:c.6687T>G	NP_001341831.1:p.Pro2229=
NM_001354903.2:c.6657T>G	NP_001341832.1:p.Pro2219=
NM_001354904.2:c.6582T>G	NP_001341833.1:p.Pro2194=
NM_001354905.2:c.6480T>G	NP_001341834.1:p.Pro2160=
NM_001354906.2:c.6111T>G	NP_001341835.1:p.Pro2037=