Canonical Allele Identifier: CA446208686

Gene: APC

Linked Data

• ClinVar Variation Id: 2084818
• ClinVar RCV Id: RCV003744849
• dbSNP Id: rs137988845
• MyVariant Identifiers: chr5:g.112176196G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840499G>T , CM000667.2:g.112840499G>T	GRCh38
NC_000005.9:g.112176196G>T , CM000667.1:g.112176196G>T	GRCh37
NC_000005.8:g.112204095G>T	NCBI36
NG_008481.4:g.152979G>T , LRG_130:g.152979G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4959G>T	ENSP00000473355.2:p.Gly1653=
ENST00000505350.2:c.*4911G>T	ENSP00000481752.1:n.*4911G>T
ENST00000507379.6:c.4851G>T	ENSP00000423224.2:p.Gly1617=
ENST00000509732.6:c.4905G>T	ENSP00000426541.2:p.Gly1635=
ENST00000512211.7:c.4905G>T	ENSP00000423828.3:p.Gly1635=
ENST00000257430.9:c.4905G>T MANE Select	ENSP00000257430.4:p.Gly1635=
ENST00000257430.8:c.4905G>T	ENSP00000257430.4:p.Gly1635=
ENST00000508376.6:c.4905G>T	ENSP00000427089.2:p.Gly1635=
ENST00000508624.5:c.*4227G>T	ENSP00000424265.1:n.*4227G>T
ENST00000520401.1:c.230+11527G>T
NM_000038.5:c.4905G>T	NP_000029.2:p.Gly1635=
NM_001127510.2:c.4905G>T	NP_001120982.1:p.Gly1635=
NM_001127511.2:c.4851G>T	NP_001120983.2:p.Gly1617=
NM_001354895.1:c.4905G>T	NP_001341824.1:p.Gly1635=
NM_001354896.1:c.4959G>T	NP_001341825.1:p.Gly1653=
NM_001354897.1:c.4935G>T	NP_001341826.1:p.Gly1645=
NM_001354898.1:c.4830G>T	NP_001341827.1:p.Gly1610=
NM_001354899.1:c.4821G>T	NP_001341828.1:p.Gly1607=
NM_001354900.1:c.4782G>T	NP_001341829.1:p.Gly1594=
NM_001354901.1:c.4728G>T	NP_001341830.1:p.Gly1576=
NM_001354902.1:c.4632G>T	NP_001341831.1:p.Gly1544=
NM_001354903.1:c.4602G>T	NP_001341832.1:p.Gly1534=
NM_001354904.1:c.4527G>T	NP_001341833.1:p.Gly1509=
NM_001354905.1:c.4425G>T	NP_001341834.1:p.Gly1475=
NM_001354906.1:c.4056G>T	NP_001341835.1:p.Gly1352=
NM_000038.6:c.4905G>T MANE Select	NP_000029.2:p.Gly1635=
NM_001127510.3:c.4905G>T	NP_001120982.1:p.Gly1635=
NM_001127511.3:c.4851G>T	NP_001120983.2:p.Gly1617=
NM_001354895.2:c.4905G>T	NP_001341824.1:p.Gly1635=
NM_001354896.2:c.4959G>T	NP_001341825.1:p.Gly1653=
NM_001354897.2:c.4935G>T	NP_001341826.1:p.Gly1645=
NM_001354898.2:c.4830G>T	NP_001341827.1:p.Gly1610=
NM_001354899.2:c.4821G>T	NP_001341828.1:p.Gly1607=
NM_001354900.2:c.4782G>T	NP_001341829.1:p.Gly1594=
NM_001354901.2:c.4728G>T	NP_001341830.1:p.Gly1576=
NM_001354902.2:c.4632G>T	NP_001341831.1:p.Gly1544=
NM_001354903.2:c.4602G>T	NP_001341832.1:p.Gly1534=
NM_001354904.2:c.4527G>T	NP_001341833.1:p.Gly1509=
NM_001354905.2:c.4425G>T	NP_001341834.1:p.Gly1475=
NM_001354906.2:c.4056G>T	NP_001341835.1:p.Gly1352=