Canonical Allele Identifier: CA891842607

Gene: APC

Linked Data

• ClinVar Variation Id: 584669
• ClinVar RCV Id: RCV000708962
• dbSNP Id: rs1561584336
• MyVariant Identifiers: chr5:g.112174665dupT (hg19) ; chr5:g.112838968dupT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838968dup , CM000667.2:g.112838968dup	GRCh38
NC_000005.9:g.112174665dup , CM000667.1:g.112174665dup	GRCh37
NC_000005.8:g.112202564dup	NCBI36
NG_008481.4:g.151448dup , LRG_130:g.151448dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3039dup	ENSP00000484935.2:n.3039dup
ENST00000504915.3:c.3428dup	ENSP00000473355.2:p.Ser1144LysfsTer9
ENST00000505350.2:c.*3380dup	ENSP00000481752.1:n.*3380dup
ENST00000507379.6:c.3320dup	ENSP00000423224.2:p.Ser1108LysfsTer9
ENST00000509732.6:c.3374dup	ENSP00000426541.2:p.Ser1126LysfsTer9
ENST00000512211.7:c.3374dup	ENSP00000423828.3:p.Ser1126LysfsTer9
ENST00000257430.9:c.3374dup MANE Select	ENSP00000257430.4:p.Ser1126LysfsTer9
ENST00000257430.8:c.3374dup	ENSP00000257430.4:p.Ser1126LysfsTer9
ENST00000502371.2:c.1727dup
ENST00000507379.5:c.3320dup	ENSP00000423224.1:p.Ser1108LysfsTer9
ENST00000508376.6:c.3374dup	ENSP00000427089.2:p.Ser1126LysfsTer9
ENST00000508624.5:c.*2696dup	ENSP00000424265.1:n.*2696dup
ENST00000512211.6:c.3374dup	ENSP00000423828.2:p.Ser1126LysfsTer9
ENST00000520401.1:c.230+9996dup
NM_000038.5:c.3374dup	NP_000029.2:p.Ser1126LysfsTer9
NM_001127510.2:c.3374dup	NP_001120982.1:p.Ser1126LysfsTer9
NM_001127511.2:c.3320dup	NP_001120983.2:p.Ser1108LysfsTer9
NM_001354895.1:c.3374dup	NP_001341824.1:p.Ser1126LysfsTer9
NM_001354896.1:c.3428dup	NP_001341825.1:p.Ser1144LysfsTer9
NM_001354897.1:c.3404dup	NP_001341826.1:p.Ser1136LysfsTer9
NM_001354898.1:c.3299dup	NP_001341827.1:p.Ser1101LysfsTer9
NM_001354899.1:c.3290dup	NP_001341828.1:p.Ser1098LysfsTer9
NM_001354900.1:c.3251dup	NP_001341829.1:p.Ser1085LysfsTer9
NM_001354901.1:c.3197dup	NP_001341830.1:p.Ser1067LysfsTer9
NM_001354902.1:c.3101dup	NP_001341831.1:p.Ser1035LysfsTer9
NM_001354903.1:c.3071dup	NP_001341832.1:p.Ser1025LysfsTer9
NM_001354904.1:c.2996dup	NP_001341833.1:p.Ser1000LysfsTer9
NM_001354905.1:c.2894dup	NP_001341834.1:p.Ser966LysfsTer9
NM_001354906.1:c.2525dup	NP_001341835.1:p.Ser843LysfsTer9
NM_000038.6:c.3374dup MANE Select	NP_000029.2:p.Ser1126LysfsTer9
NM_001127510.3:c.3374dup	NP_001120982.1:p.Ser1126LysfsTer9
NM_001127511.3:c.3320dup	NP_001120983.2:p.Ser1108LysfsTer9
NM_001354895.2:c.3374dup	NP_001341824.1:p.Ser1126LysfsTer9
NM_001354896.2:c.3428dup	NP_001341825.1:p.Ser1144LysfsTer9
NM_001354897.2:c.3404dup	NP_001341826.1:p.Ser1136LysfsTer9
NM_001354898.2:c.3299dup	NP_001341827.1:p.Ser1101LysfsTer9
NM_001354899.2:c.3290dup	NP_001341828.1:p.Ser1098LysfsTer9
NM_001354900.2:c.3251dup	NP_001341829.1:p.Ser1085LysfsTer9
NM_001354901.2:c.3197dup	NP_001341830.1:p.Ser1067LysfsTer9
NM_001354902.2:c.3101dup	NP_001341831.1:p.Ser1035LysfsTer9
NM_001354903.2:c.3071dup	NP_001341832.1:p.Ser1025LysfsTer9
NM_001354904.2:c.2996dup	NP_001341833.1:p.Ser1000LysfsTer9
NM_001354905.2:c.2894dup	NP_001341834.1:p.Ser966LysfsTer9
NM_001354906.2:c.2525dup	NP_001341835.1:p.Ser843LysfsTer9