Canonical Allele Identifier: CA2695204974

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839403_112839404insC , CM000667.2:g.112839403_112839404insC	GRCh38
NC_000005.9:g.112175100_112175101insC , CM000667.1:g.112175100_112175101insC	GRCh37
NC_000005.8:g.112202999_112203000insC	NCBI36
NG_008481.4:g.151883_151884insC , LRG_130:g.151883_151884insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3474_3475insC	ENSP00000484935.2:n.3474_3475insC
ENST00000504915.3:c.3863_3864insC	ENSP00000473355.2:p.Ser1290PhefsTer4
ENST00000505350.2:c.*3815_*3816insC	ENSP00000481752.1:n.*3815_*3816insC
ENST00000507379.6:c.3755_3756insC	ENSP00000423224.2:p.Ser1254PhefsTer4
ENST00000509732.6:c.3809_3810insC	ENSP00000426541.2:p.Ser1272PhefsTer4
ENST00000512211.7:c.3809_3810insC	ENSP00000423828.3:p.Ser1272PhefsTer4
ENST00000257430.9:c.3809_3810insC MANE Select	ENSP00000257430.4:p.Ser1272PhefsTer4
ENST00000257430.8:c.3809_3810insC	ENSP00000257430.4:p.Ser1272PhefsTer4
ENST00000502371.2:c.2162_2163insC
ENST00000508376.6:c.3809_3810insC	ENSP00000427089.2:p.Ser1272PhefsTer4
ENST00000508624.5:c.*3131_*3132insC	ENSP00000424265.1:n.*3131_*3132insC
ENST00000512211.6:c.3809_3810insC	ENSP00000423828.2:p.Ser1272PhefsTer4
ENST00000520401.1:c.230+10431_230+10432insC
NM_000038.5:c.3809_3810insC	NP_000029.2:p.Ser1272PhefsTer4
NM_001127510.2:c.3809_3810insC	NP_001120982.1:p.Ser1272PhefsTer4
NM_001127511.2:c.3755_3756insC	NP_001120983.2:p.Ser1254PhefsTer4
NM_001354895.1:c.3809_3810insC	NP_001341824.1:p.Ser1272PhefsTer4
NM_001354896.1:c.3863_3864insC	NP_001341825.1:p.Ser1290PhefsTer4
NM_001354897.1:c.3839_3840insC	NP_001341826.1:p.Ser1282PhefsTer4
NM_001354898.1:c.3734_3735insC	NP_001341827.1:p.Ser1247PhefsTer4
NM_001354899.1:c.3725_3726insC	NP_001341828.1:p.Ser1244PhefsTer4
NM_001354900.1:c.3686_3687insC	NP_001341829.1:p.Ser1231PhefsTer4
NM_001354901.1:c.3632_3633insC	NP_001341830.1:p.Ser1213PhefsTer4
NM_001354902.1:c.3536_3537insC	NP_001341831.1:p.Ser1181PhefsTer4
NM_001354903.1:c.3506_3507insC	NP_001341832.1:p.Ser1171PhefsTer4
NM_001354904.1:c.3431_3432insC	NP_001341833.1:p.Ser1146PhefsTer4
NM_001354905.1:c.3329_3330insC	NP_001341834.1:p.Ser1112PhefsTer4
NM_001354906.1:c.2960_2961insC	NP_001341835.1:p.Ser989PhefsTer4
NM_000038.6:c.3809_3810insC MANE Select	NP_000029.2:p.Ser1272PhefsTer4
NM_001127510.3:c.3809_3810insC	NP_001120982.1:p.Ser1272PhefsTer4
NM_001127511.3:c.3755_3756insC	NP_001120983.2:p.Ser1254PhefsTer4
NM_001354895.2:c.3809_3810insC	NP_001341824.1:p.Ser1272PhefsTer4
NM_001354896.2:c.3863_3864insC	NP_001341825.1:p.Ser1290PhefsTer4
NM_001354897.2:c.3839_3840insC	NP_001341826.1:p.Ser1282PhefsTer4
NM_001354898.2:c.3734_3735insC	NP_001341827.1:p.Ser1247PhefsTer4
NM_001354899.2:c.3725_3726insC	NP_001341828.1:p.Ser1244PhefsTer4
NM_001354900.2:c.3686_3687insC	NP_001341829.1:p.Ser1231PhefsTer4
NM_001354901.2:c.3632_3633insC	NP_001341830.1:p.Ser1213PhefsTer4
NM_001354902.2:c.3536_3537insC	NP_001341831.1:p.Ser1181PhefsTer4
NM_001354903.2:c.3506_3507insC	NP_001341832.1:p.Ser1171PhefsTer4
NM_001354904.2:c.3431_3432insC	NP_001341833.1:p.Ser1146PhefsTer4
NM_001354905.2:c.3329_3330insC	NP_001341834.1:p.Ser1112PhefsTer4
NM_001354906.2:c.2960_2961insC	NP_001341835.1:p.Ser989PhefsTer4