Canonical Allele Identifier: CA1573470667

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840262T= , CM000667.2:g.112840262T=	GRCh38
NC_000005.9:g.112175959T= , CM000667.1:g.112175959T=	GRCh37
NC_000005.8:g.112203858T=	NCBI36
NG_008481.4:g.152742T= , LRG_130:g.152742T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4722T=	ENSP00000473355.2:p.Thr1574=
ENST00000505350.2:c.*4674T=	ENSP00000481752.1:n.*4674T=
ENST00000507379.6:c.4614T=	ENSP00000423224.2:p.Thr1538=
ENST00000509732.6:c.4668T=	ENSP00000426541.2:p.Thr1556=
ENST00000512211.7:c.4668T=	ENSP00000423828.3:p.Thr1556=
ENST00000257430.9:c.4668T= MANE Select	ENSP00000257430.4:p.Thr1556=
ENST00000257430.8:c.4668T=	ENSP00000257430.4:p.Thr1556=
ENST00000508376.6:c.4668T=	ENSP00000427089.2:p.Thr1556=
ENST00000508624.5:c.*3990T=	ENSP00000424265.1:n.*3990T=
ENST00000520401.1:c.230+11290T=
NM_000038.5:c.4668T=	NP_000029.2:p.Thr1556=
NM_001127510.2:c.4668T=	NP_001120982.1:p.Thr1556=
NM_001127511.2:c.4614T=	NP_001120983.2:p.Thr1538=
NM_001354895.1:c.4668T=	NP_001341824.1:p.Thr1556=
NM_001354896.1:c.4722T=	NP_001341825.1:p.Thr1574=
NM_001354897.1:c.4698T=	NP_001341826.1:p.Thr1566=
NM_001354898.1:c.4593T=	NP_001341827.1:p.Thr1531=
NM_001354899.1:c.4584T=	NP_001341828.1:p.Thr1528=
NM_001354900.1:c.4545T=	NP_001341829.1:p.Thr1515=
NM_001354901.1:c.4491T=	NP_001341830.1:p.Thr1497=
NM_001354902.1:c.4395T=	NP_001341831.1:p.Thr1465=
NM_001354903.1:c.4365T=	NP_001341832.1:p.Thr1455=
NM_001354904.1:c.4290T=	NP_001341833.1:p.Thr1430=
NM_001354905.1:c.4188T=	NP_001341834.1:p.Thr1396=
NM_001354906.1:c.3819T=	NP_001341835.1:p.Thr1273=
NM_000038.6:c.4668T= MANE Select	NP_000029.2:p.Thr1556=
NM_001127510.3:c.4668T=	NP_001120982.1:p.Thr1556=
NM_001127511.3:c.4614T=	NP_001120983.2:p.Thr1538=
NM_001354895.2:c.4668T=	NP_001341824.1:p.Thr1556=
NM_001354896.2:c.4722T=	NP_001341825.1:p.Thr1574=
NM_001354897.2:c.4698T=	NP_001341826.1:p.Thr1566=
NM_001354898.2:c.4593T=	NP_001341827.1:p.Thr1531=
NM_001354899.2:c.4584T=	NP_001341828.1:p.Thr1528=
NM_001354900.2:c.4545T=	NP_001341829.1:p.Thr1515=
NM_001354901.2:c.4491T=	NP_001341830.1:p.Thr1497=
NM_001354902.2:c.4395T=	NP_001341831.1:p.Thr1465=
NM_001354903.2:c.4365T=	NP_001341832.1:p.Thr1455=
NM_001354904.2:c.4290T=	NP_001341833.1:p.Thr1430=
NM_001354905.2:c.4188T=	NP_001341834.1:p.Thr1396=
NM_001354906.2:c.3819T=	NP_001341835.1:p.Thr1273=