Canonical Allele Identifier: CA446206697

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176021_112176022insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840325dup , CM000667.2:g.112840325dup	GRCh38
NC_000005.9:g.112176022dup , CM000667.1:g.112176022dup	GRCh37
NC_000005.8:g.112203921dup	NCBI36
NG_008481.4:g.152805dup , LRG_130:g.152805dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4785dup	ENSP00000473355.2:p.Cys1596MetfsTer13
ENST00000505350.2:c.*4737dup	ENSP00000481752.1:n.*4737dup
ENST00000507379.6:c.4677dup	ENSP00000423224.2:p.Cys1560MetfsTer13
ENST00000509732.6:c.4731dup	ENSP00000426541.2:p.Cys1578MetfsTer13
ENST00000512211.7:c.4731dup	ENSP00000423828.3:p.Cys1578MetfsTer13
ENST00000257430.9:c.4731dup MANE Select	ENSP00000257430.4:p.Cys1578MetfsTer13
ENST00000257430.8:c.4731dup	ENSP00000257430.4:p.Cys1578MetfsTer13
ENST00000508376.6:c.4731dup	ENSP00000427089.2:p.Cys1578MetfsTer13
ENST00000508624.5:c.*4053dup	ENSP00000424265.1:n.*4053dup
ENST00000520401.1:c.230+11353dup
NM_000038.5:c.4731dup	NP_000029.2:p.Cys1578MetfsTer13
NM_001127510.2:c.4731dup	NP_001120982.1:p.Cys1578MetfsTer13
NM_001127511.2:c.4677dup	NP_001120983.2:p.Cys1560MetfsTer13
NM_001354895.1:c.4731dup	NP_001341824.1:p.Cys1578MetfsTer13
NM_001354896.1:c.4785dup	NP_001341825.1:p.Cys1596MetfsTer13
NM_001354897.1:c.4761dup	NP_001341826.1:p.Cys1588MetfsTer13
NM_001354898.1:c.4656dup	NP_001341827.1:p.Cys1553MetfsTer13
NM_001354899.1:c.4647dup	NP_001341828.1:p.Cys1550MetfsTer13
NM_001354900.1:c.4608dup	NP_001341829.1:p.Cys1537MetfsTer13
NM_001354901.1:c.4554dup	NP_001341830.1:p.Cys1519MetfsTer13
NM_001354902.1:c.4458dup	NP_001341831.1:p.Cys1487MetfsTer13
NM_001354903.1:c.4428dup	NP_001341832.1:p.Cys1477MetfsTer13
NM_001354904.1:c.4353dup	NP_001341833.1:p.Cys1452MetfsTer13
NM_001354905.1:c.4251dup	NP_001341834.1:p.Cys1418MetfsTer13
NM_001354906.1:c.3882dup	NP_001341835.1:p.Cys1295MetfsTer13
NM_000038.6:c.4731dup MANE Select	NP_000029.2:p.Cys1578MetfsTer13
NM_001127510.3:c.4731dup	NP_001120982.1:p.Cys1578MetfsTer13
NM_001127511.3:c.4677dup	NP_001120983.2:p.Cys1560MetfsTer13
NM_001354895.2:c.4731dup	NP_001341824.1:p.Cys1578MetfsTer13
NM_001354896.2:c.4785dup	NP_001341825.1:p.Cys1596MetfsTer13
NM_001354897.2:c.4761dup	NP_001341826.1:p.Cys1588MetfsTer13
NM_001354898.2:c.4656dup	NP_001341827.1:p.Cys1553MetfsTer13
NM_001354899.2:c.4647dup	NP_001341828.1:p.Cys1550MetfsTer13
NM_001354900.2:c.4608dup	NP_001341829.1:p.Cys1537MetfsTer13
NM_001354901.2:c.4554dup	NP_001341830.1:p.Cys1519MetfsTer13
NM_001354902.2:c.4458dup	NP_001341831.1:p.Cys1487MetfsTer13
NM_001354903.2:c.4428dup	NP_001341832.1:p.Cys1477MetfsTer13
NM_001354904.2:c.4353dup	NP_001341833.1:p.Cys1452MetfsTer13
NM_001354905.2:c.4251dup	NP_001341834.1:p.Cys1418MetfsTer13
NM_001354906.2:c.3882dup	NP_001341835.1:p.Cys1295MetfsTer13