Canonical Allele Identifier: CA446208688

Gene: APC

Linked Data

• dbSNP Id: rs2149927148
• MyVariant Identifiers: chr5:g.112176202T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840505T>C , CM000667.2:g.112840505T>C	GRCh38
NC_000005.9:g.112176202T>C , CM000667.1:g.112176202T>C	GRCh37
NC_000005.8:g.112204101T>C	NCBI36
NG_008481.4:g.152985T>C , LRG_130:g.152985T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4965T>C	ENSP00000473355.2:p.Asp1655=
ENST00000505350.2:c.*4917T>C	ENSP00000481752.1:n.*4917T>C
ENST00000507379.6:c.4857T>C	ENSP00000423224.2:p.Asp1619=
ENST00000509732.6:c.4911T>C	ENSP00000426541.2:p.Asp1637=
ENST00000512211.7:c.4911T>C	ENSP00000423828.3:p.Asp1637=
ENST00000257430.9:c.4911T>C MANE Select	ENSP00000257430.4:p.Asp1637=
ENST00000257430.8:c.4911T>C	ENSP00000257430.4:p.Asp1637=
ENST00000508376.6:c.4911T>C	ENSP00000427089.2:p.Asp1637=
ENST00000508624.5:c.*4233T>C	ENSP00000424265.1:n.*4233T>C
ENST00000520401.1:c.230+11533T>C
NM_000038.5:c.4911T>C	NP_000029.2:p.Asp1637=
NM_001127510.2:c.4911T>C	NP_001120982.1:p.Asp1637=
NM_001127511.2:c.4857T>C	NP_001120983.2:p.Asp1619=
NM_001354895.1:c.4911T>C	NP_001341824.1:p.Asp1637=
NM_001354896.1:c.4965T>C	NP_001341825.1:p.Asp1655=
NM_001354897.1:c.4941T>C	NP_001341826.1:p.Asp1647=
NM_001354898.1:c.4836T>C	NP_001341827.1:p.Asp1612=
NM_001354899.1:c.4827T>C	NP_001341828.1:p.Asp1609=
NM_001354900.1:c.4788T>C	NP_001341829.1:p.Asp1596=
NM_001354901.1:c.4734T>C	NP_001341830.1:p.Asp1578=
NM_001354902.1:c.4638T>C	NP_001341831.1:p.Asp1546=
NM_001354903.1:c.4608T>C	NP_001341832.1:p.Asp1536=
NM_001354904.1:c.4533T>C	NP_001341833.1:p.Asp1511=
NM_001354905.1:c.4431T>C	NP_001341834.1:p.Asp1477=
NM_001354906.1:c.4062T>C	NP_001341835.1:p.Asp1354=
NM_000038.6:c.4911T>C MANE Select	NP_000029.2:p.Asp1637=
NM_001127510.3:c.4911T>C	NP_001120982.1:p.Asp1637=
NM_001127511.3:c.4857T>C	NP_001120983.2:p.Asp1619=
NM_001354895.2:c.4911T>C	NP_001341824.1:p.Asp1637=
NM_001354896.2:c.4965T>C	NP_001341825.1:p.Asp1655=
NM_001354897.2:c.4941T>C	NP_001341826.1:p.Asp1647=
NM_001354898.2:c.4836T>C	NP_001341827.1:p.Asp1612=
NM_001354899.2:c.4827T>C	NP_001341828.1:p.Asp1609=
NM_001354900.2:c.4788T>C	NP_001341829.1:p.Asp1596=
NM_001354901.2:c.4734T>C	NP_001341830.1:p.Asp1578=
NM_001354902.2:c.4638T>C	NP_001341831.1:p.Asp1546=
NM_001354903.2:c.4608T>C	NP_001341832.1:p.Asp1536=
NM_001354904.2:c.4533T>C	NP_001341833.1:p.Asp1511=
NM_001354905.2:c.4431T>C	NP_001341834.1:p.Asp1477=
NM_001354906.2:c.4062T>C	NP_001341835.1:p.Asp1354=