Canonical Allele Identifier: CA16032464

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176384A>C (hg19) ; chr5:g.112840687A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840687A>C , CM000667.2:g.112840687A>C	GRCh38
NC_000005.9:g.112176384A>C , CM000667.1:g.112176384A>C	GRCh37
NC_000005.8:g.112204283A>C	NCBI36
NG_008481.4:g.153167A>C , LRG_130:g.153167A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5147A>C	ENSP00000473355.2:p.Asp1716Ala
ENST00000505350.2:c.*5099A>C	ENSP00000481752.1:n.*5099A>C
ENST00000507379.6:c.5039A>C	ENSP00000423224.2:p.Asp1680Ala
ENST00000509732.6:c.5093A>C	ENSP00000426541.2:p.Asp1698Ala
ENST00000512211.7:c.5093A>C	ENSP00000423828.3:p.Asp1698Ala
ENST00000257430.9:c.5093A>C MANE Select	ENSP00000257430.4:p.Asp1698Ala
ENST00000257430.8:c.5093A>C	ENSP00000257430.4:p.Asp1698Ala
ENST00000508376.6:c.5093A>C	ENSP00000427089.2:p.Asp1698Ala
ENST00000508624.5:c.*4415A>C	ENSP00000424265.1:n.*4415A>C
ENST00000520401.1:c.230+11715A>C
NM_000038.5:c.5093A>C	NP_000029.2:p.Asp1698Ala
NM_001127510.2:c.5093A>C	NP_001120982.1:p.Asp1698Ala
NM_001127511.2:c.5039A>C	NP_001120983.2:p.Asp1680Ala
NM_001354895.1:c.5093A>C	NP_001341824.1:p.Asp1698Ala
NM_001354896.1:c.5147A>C	NP_001341825.1:p.Asp1716Ala
NM_001354897.1:c.5123A>C	NP_001341826.1:p.Asp1708Ala
NM_001354898.1:c.5018A>C	NP_001341827.1:p.Asp1673Ala
NM_001354899.1:c.5009A>C	NP_001341828.1:p.Asp1670Ala
NM_001354900.1:c.4970A>C	NP_001341829.1:p.Asp1657Ala
NM_001354901.1:c.4916A>C	NP_001341830.1:p.Asp1639Ala
NM_001354902.1:c.4820A>C	NP_001341831.1:p.Asp1607Ala
NM_001354903.1:c.4790A>C	NP_001341832.1:p.Asp1597Ala
NM_001354904.1:c.4715A>C	NP_001341833.1:p.Asp1572Ala
NM_001354905.1:c.4613A>C	NP_001341834.1:p.Asp1538Ala
NM_001354906.1:c.4244A>C	NP_001341835.1:p.Asp1415Ala
NM_000038.6:c.5093A>C MANE Select	NP_000029.2:p.Asp1698Ala
NM_001127510.3:c.5093A>C	NP_001120982.1:p.Asp1698Ala
NM_001127511.3:c.5039A>C	NP_001120983.2:p.Asp1680Ala
NM_001354895.2:c.5093A>C	NP_001341824.1:p.Asp1698Ala
NM_001354896.2:c.5147A>C	NP_001341825.1:p.Asp1716Ala
NM_001354897.2:c.5123A>C	NP_001341826.1:p.Asp1708Ala
NM_001354898.2:c.5018A>C	NP_001341827.1:p.Asp1673Ala
NM_001354899.2:c.5009A>C	NP_001341828.1:p.Asp1670Ala
NM_001354900.2:c.4970A>C	NP_001341829.1:p.Asp1657Ala
NM_001354901.2:c.4916A>C	NP_001341830.1:p.Asp1639Ala
NM_001354902.2:c.4820A>C	NP_001341831.1:p.Asp1607Ala
NM_001354903.2:c.4790A>C	NP_001341832.1:p.Asp1597Ala
NM_001354904.2:c.4715A>C	NP_001341833.1:p.Asp1572Ala
NM_001354905.2:c.4613A>C	NP_001341834.1:p.Asp1538Ala
NM_001354906.2:c.4244A>C	NP_001341835.1:p.Asp1415Ala