Canonical Allele Identifier: CA16028002

Gene: APC

Linked Data

• ClinVar Variation Id: 1315725
• ClinVar RCV Id: RCV001755387 ; RCV002449419 ; RCV003653489
• dbSNP Id: rs1765323229
• MyVariant Identifiers: chr5:g.112174337G>T (hg19) ; chr5:g.112838640G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838640G>T , CM000667.2:g.112838640G>T	GRCh38
NC_000005.9:g.112174337G>T , CM000667.1:g.112174337G>T	GRCh37
NC_000005.8:g.112202236G>T	NCBI36
NG_008481.4:g.151120G>T , LRG_130:g.151120G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2711G>T	ENSP00000484935.2:n.2711G>T
ENST00000504915.3:c.3100G>T	ENSP00000473355.2:p.Asp1034Tyr
ENST00000505350.2:c.*3052G>T	ENSP00000481752.1:n.*3052G>T
ENST00000507379.6:c.2992G>T	ENSP00000423224.2:p.Asp998Tyr
ENST00000509732.6:c.3046G>T	ENSP00000426541.2:p.Asp1016Tyr
ENST00000512211.7:c.3046G>T	ENSP00000423828.3:p.Asp1016Tyr
ENST00000257430.9:c.3046G>T MANE Select	ENSP00000257430.4:p.Asp1016Tyr
ENST00000257430.8:c.3046G>T	ENSP00000257430.4:p.Asp1016Tyr
ENST00000502371.2:c.1399G>T
ENST00000507379.5:c.2992G>T	ENSP00000423224.1:p.Asp998Tyr
ENST00000508376.6:c.3046G>T	ENSP00000427089.2:p.Asp1016Tyr
ENST00000508624.5:c.*2368G>T	ENSP00000424265.1:n.*2368G>T
ENST00000512211.6:c.3046G>T	ENSP00000423828.2:p.Asp1016Tyr
ENST00000520401.1:c.230+9668G>T
NM_000038.5:c.3046G>T	NP_000029.2:p.Asp1016Tyr
NM_001127510.2:c.3046G>T	NP_001120982.1:p.Asp1016Tyr
NM_001127511.2:c.2992G>T	NP_001120983.2:p.Asp998Tyr
NM_001354895.1:c.3046G>T	NP_001341824.1:p.Asp1016Tyr
NM_001354896.1:c.3100G>T	NP_001341825.1:p.Asp1034Tyr
NM_001354897.1:c.3076G>T	NP_001341826.1:p.Asp1026Tyr
NM_001354898.1:c.2971G>T	NP_001341827.1:p.Asp991Tyr
NM_001354899.1:c.2962G>T	NP_001341828.1:p.Asp988Tyr
NM_001354900.1:c.2923G>T	NP_001341829.1:p.Asp975Tyr
NM_001354901.1:c.2869G>T	NP_001341830.1:p.Asp957Tyr
NM_001354902.1:c.2773G>T	NP_001341831.1:p.Asp925Tyr
NM_001354903.1:c.2743G>T	NP_001341832.1:p.Asp915Tyr
NM_001354904.1:c.2668G>T	NP_001341833.1:p.Asp890Tyr
NM_001354905.1:c.2566G>T	NP_001341834.1:p.Asp856Tyr
NM_001354906.1:c.2197G>T	NP_001341835.1:p.Asp733Tyr
NM_000038.6:c.3046G>T MANE Select	NP_000029.2:p.Asp1016Tyr
NM_001127510.3:c.3046G>T	NP_001120982.1:p.Asp1016Tyr
NM_001127511.3:c.2992G>T	NP_001120983.2:p.Asp998Tyr
NM_001354895.2:c.3046G>T	NP_001341824.1:p.Asp1016Tyr
NM_001354896.2:c.3100G>T	NP_001341825.1:p.Asp1034Tyr
NM_001354897.2:c.3076G>T	NP_001341826.1:p.Asp1026Tyr
NM_001354898.2:c.2971G>T	NP_001341827.1:p.Asp991Tyr
NM_001354899.2:c.2962G>T	NP_001341828.1:p.Asp988Tyr
NM_001354900.2:c.2923G>T	NP_001341829.1:p.Asp975Tyr
NM_001354901.2:c.2869G>T	NP_001341830.1:p.Asp957Tyr
NM_001354902.2:c.2773G>T	NP_001341831.1:p.Asp925Tyr
NM_001354903.2:c.2743G>T	NP_001341832.1:p.Asp915Tyr
NM_001354904.2:c.2668G>T	NP_001341833.1:p.Asp890Tyr
NM_001354905.2:c.2566G>T	NP_001341834.1:p.Asp856Tyr
NM_001354906.2:c.2197G>T	NP_001341835.1:p.Asp733Tyr