Canonical Allele Identifier: CA446208758

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176304T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840607T>A , CM000667.2:g.112840607T>A	GRCh38
NC_000005.9:g.112176304T>A , CM000667.1:g.112176304T>A	GRCh37
NC_000005.8:g.112204203T>A	NCBI36
NG_008481.4:g.153087T>A , LRG_130:g.153087T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5067T>A	ENSP00000473355.2:p.Ala1689=
ENST00000505350.2:c.*5019T>A	ENSP00000481752.1:n.*5019T>A
ENST00000507379.6:c.4959T>A	ENSP00000423224.2:p.Ala1653=
ENST00000509732.6:c.5013T>A	ENSP00000426541.2:p.Ala1671=
ENST00000512211.7:c.5013T>A	ENSP00000423828.3:p.Ala1671=
ENST00000257430.9:c.5013T>A MANE Select	ENSP00000257430.4:p.Ala1671=
ENST00000257430.8:c.5013T>A	ENSP00000257430.4:p.Ala1671=
ENST00000508376.6:c.5013T>A	ENSP00000427089.2:p.Ala1671=
ENST00000508624.5:c.*4335T>A	ENSP00000424265.1:n.*4335T>A
ENST00000520401.1:c.230+11635T>A
NM_000038.5:c.5013T>A	NP_000029.2:p.Ala1671=
NM_001127510.2:c.5013T>A	NP_001120982.1:p.Ala1671=
NM_001127511.2:c.4959T>A	NP_001120983.2:p.Ala1653=
NM_001354895.1:c.5013T>A	NP_001341824.1:p.Ala1671=
NM_001354896.1:c.5067T>A	NP_001341825.1:p.Ala1689=
NM_001354897.1:c.5043T>A	NP_001341826.1:p.Ala1681=
NM_001354898.1:c.4938T>A	NP_001341827.1:p.Ala1646=
NM_001354899.1:c.4929T>A	NP_001341828.1:p.Ala1643=
NM_001354900.1:c.4890T>A	NP_001341829.1:p.Ala1630=
NM_001354901.1:c.4836T>A	NP_001341830.1:p.Ala1612=
NM_001354902.1:c.4740T>A	NP_001341831.1:p.Ala1580=
NM_001354903.1:c.4710T>A	NP_001341832.1:p.Ala1570=
NM_001354904.1:c.4635T>A	NP_001341833.1:p.Ala1545=
NM_001354905.1:c.4533T>A	NP_001341834.1:p.Ala1511=
NM_001354906.1:c.4164T>A	NP_001341835.1:p.Ala1388=
NM_000038.6:c.5013T>A MANE Select	NP_000029.2:p.Ala1671=
NM_001127510.3:c.5013T>A	NP_001120982.1:p.Ala1671=
NM_001127511.3:c.4959T>A	NP_001120983.2:p.Ala1653=
NM_001354895.2:c.5013T>A	NP_001341824.1:p.Ala1671=
NM_001354896.2:c.5067T>A	NP_001341825.1:p.Ala1689=
NM_001354897.2:c.5043T>A	NP_001341826.1:p.Ala1681=
NM_001354898.2:c.4938T>A	NP_001341827.1:p.Ala1646=
NM_001354899.2:c.4929T>A	NP_001341828.1:p.Ala1643=
NM_001354900.2:c.4890T>A	NP_001341829.1:p.Ala1630=
NM_001354901.2:c.4836T>A	NP_001341830.1:p.Ala1612=
NM_001354902.2:c.4740T>A	NP_001341831.1:p.Ala1580=
NM_001354903.2:c.4710T>A	NP_001341832.1:p.Ala1570=
NM_001354904.2:c.4635T>A	NP_001341833.1:p.Ala1545=
NM_001354905.2:c.4533T>A	NP_001341834.1:p.Ala1511=
NM_001354906.2:c.4164T>A	NP_001341835.1:p.Ala1388=