Canonical Allele Identifier: CA16027732

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838524G>A , CM000667.2:g.112838524G>A	GRCh38
NC_000005.9:g.112174221G>A , CM000667.1:g.112174221G>A	GRCh37
NC_000005.8:g.112202120G>A	NCBI36
NG_008481.4:g.151004G>A , LRG_130:g.151004G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.2930G>A MANE Select	NP_000029.2:p.Gly977Asp
ENST00000257430.9:c.2930G>A MANE Select	ENSP00000257430.4:p.Gly977Asp
NM_000038.5:c.2930G>A	NP_000029.2:p.Gly977Asp
NM_001127510.2:c.2930G>A	NP_001120982.1:p.Gly977Asp
NM_001127510.3:c.2930G>A	NP_001120982.1:p.Gly977Asp
NM_001127511.2:c.2876G>A	NP_001120983.2:p.Gly959Asp
NM_001127511.3:c.2876G>A	NP_001120983.2:p.Gly959Asp
NM_001354895.1:c.2930G>A	NP_001341824.1:p.Gly977Asp
NM_001354895.2:c.2930G>A	NP_001341824.1:p.Gly977Asp
NM_001354896.1:c.2984G>A	NP_001341825.1:p.Gly995Asp
NM_001354896.2:c.2984G>A	NP_001341825.1:p.Gly995Asp
NM_001354897.1:c.2960G>A	NP_001341826.1:p.Gly987Asp
NM_001354897.2:c.2960G>A	NP_001341826.1:p.Gly987Asp
NM_001354898.1:c.2855G>A	NP_001341827.1:p.Gly952Asp
NM_001354898.2:c.2855G>A	NP_001341827.1:p.Gly952Asp
NM_001354899.1:c.2846G>A	NP_001341828.1:p.Gly949Asp
NM_001354899.2:c.2846G>A	NP_001341828.1:p.Gly949Asp
NM_001354900.1:c.2807G>A	NP_001341829.1:p.Gly936Asp
NM_001354900.2:c.2807G>A	NP_001341829.1:p.Gly936Asp
NM_001354901.1:c.2753G>A	NP_001341830.1:p.Gly918Asp
NM_001354901.2:c.2753G>A	NP_001341830.1:p.Gly918Asp
NM_001354902.1:c.2657G>A	NP_001341831.1:p.Gly886Asp
NM_001354902.2:c.2657G>A	NP_001341831.1:p.Gly886Asp
NM_001354903.1:c.2627G>A	NP_001341832.1:p.Gly876Asp
NM_001354903.2:c.2627G>A	NP_001341832.1:p.Gly876Asp
NM_001354904.1:c.2552G>A	NP_001341833.1:p.Gly851Asp
NM_001354904.2:c.2552G>A	NP_001341833.1:p.Gly851Asp
NM_001354905.1:c.2450G>A	NP_001341834.1:p.Gly817Asp
NM_001354905.2:c.2450G>A	NP_001341834.1:p.Gly817Asp
NM_001354906.1:c.2081G>A	NP_001341835.1:p.Gly694Asp
NM_001354906.2:c.2081G>A	NP_001341835.1:p.Gly694Asp
ENST00000257430.8:c.2930G>A	ENSP00000257430.4:p.Gly977Asp
ENST00000502371.2:c.1283G>A
ENST00000502371.3:c.2595G>A	ENSP00000484935.2:n.2595G>A
ENST00000504915.3:c.2984G>A	ENSP00000473355.2:p.Gly995Asp
ENST00000505350.2:c.*2936G>A	ENSP00000481752.1:n.*2936G>A
ENST00000507379.5:c.2876G>A	ENSP00000423224.1:p.Gly959Asp
ENST00000507379.6:c.2876G>A	ENSP00000423224.2:p.Gly959Asp
ENST00000508376.6:c.2930G>A	ENSP00000427089.2:p.Gly977Asp
ENST00000508624.5:c.*2252G>A	ENSP00000424265.1:n.*2252G>A
ENST00000509732.6:c.2930G>A	ENSP00000426541.2:p.Gly977Asp
ENST00000512211.6:c.2930G>A	ENSP00000423828.2:p.Gly977Asp
ENST00000512211.7:c.2930G>A	ENSP00000423828.3:p.Gly977Asp
ENST00000520401.1:c.230+9552G>A