Canonical Allele Identifier: CA16028793

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174695A>C (hg19) ; chr5:g.112838998A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838998A>C , CM000667.2:g.112838998A>C	GRCh38
NC_000005.9:g.112174695A>C , CM000667.1:g.112174695A>C	GRCh37
NC_000005.8:g.112202594A>C	NCBI36
NG_008481.4:g.151478A>C , LRG_130:g.151478A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3069A>C	ENSP00000484935.2:n.3069A>C
ENST00000504915.3:c.3458A>C	ENSP00000473355.2:p.Tyr1153Ser
ENST00000505350.2:c.*3410A>C	ENSP00000481752.1:n.*3410A>C
ENST00000507379.6:c.3350A>C	ENSP00000423224.2:p.Tyr1117Ser
ENST00000509732.6:c.3404A>C	ENSP00000426541.2:p.Tyr1135Ser
ENST00000512211.7:c.3404A>C	ENSP00000423828.3:p.Tyr1135Ser
ENST00000257430.9:c.3404A>C MANE Select	ENSP00000257430.4:p.Tyr1135Ser
ENST00000257430.8:c.3404A>C	ENSP00000257430.4:p.Tyr1135Ser
ENST00000502371.2:c.1757A>C
ENST00000507379.5:c.3350A>C	ENSP00000423224.1:p.Tyr1117Ser
ENST00000508376.6:c.3404A>C	ENSP00000427089.2:p.Tyr1135Ser
ENST00000508624.5:c.*2726A>C	ENSP00000424265.1:n.*2726A>C
ENST00000512211.6:c.3404A>C	ENSP00000423828.2:p.Tyr1135Ser
ENST00000520401.1:c.230+10026A>C
NM_000038.5:c.3404A>C	NP_000029.2:p.Tyr1135Ser
NM_001127510.2:c.3404A>C	NP_001120982.1:p.Tyr1135Ser
NM_001127511.2:c.3350A>C	NP_001120983.2:p.Tyr1117Ser
NM_001354895.1:c.3404A>C	NP_001341824.1:p.Tyr1135Ser
NM_001354896.1:c.3458A>C	NP_001341825.1:p.Tyr1153Ser
NM_001354897.1:c.3434A>C	NP_001341826.1:p.Tyr1145Ser
NM_001354898.1:c.3329A>C	NP_001341827.1:p.Tyr1110Ser
NM_001354899.1:c.3320A>C	NP_001341828.1:p.Tyr1107Ser
NM_001354900.1:c.3281A>C	NP_001341829.1:p.Tyr1094Ser
NM_001354901.1:c.3227A>C	NP_001341830.1:p.Tyr1076Ser
NM_001354902.1:c.3131A>C	NP_001341831.1:p.Tyr1044Ser
NM_001354903.1:c.3101A>C	NP_001341832.1:p.Tyr1034Ser
NM_001354904.1:c.3026A>C	NP_001341833.1:p.Tyr1009Ser
NM_001354905.1:c.2924A>C	NP_001341834.1:p.Tyr975Ser
NM_001354906.1:c.2555A>C	NP_001341835.1:p.Tyr852Ser
NM_000038.6:c.3404A>C MANE Select	NP_000029.2:p.Tyr1135Ser
NM_001127510.3:c.3404A>C	NP_001120982.1:p.Tyr1135Ser
NM_001127511.3:c.3350A>C	NP_001120983.2:p.Tyr1117Ser
NM_001354895.2:c.3404A>C	NP_001341824.1:p.Tyr1135Ser
NM_001354896.2:c.3458A>C	NP_001341825.1:p.Tyr1153Ser
NM_001354897.2:c.3434A>C	NP_001341826.1:p.Tyr1145Ser
NM_001354898.2:c.3329A>C	NP_001341827.1:p.Tyr1110Ser
NM_001354899.2:c.3320A>C	NP_001341828.1:p.Tyr1107Ser
NM_001354900.2:c.3281A>C	NP_001341829.1:p.Tyr1094Ser
NM_001354901.2:c.3227A>C	NP_001341830.1:p.Tyr1076Ser
NM_001354902.2:c.3131A>C	NP_001341831.1:p.Tyr1044Ser
NM_001354903.2:c.3101A>C	NP_001341832.1:p.Tyr1034Ser
NM_001354904.2:c.3026A>C	NP_001341833.1:p.Tyr1009Ser
NM_001354905.2:c.2924A>C	NP_001341834.1:p.Tyr975Ser
NM_001354906.2:c.2555A>C	NP_001341835.1:p.Tyr852Ser