Canonical Allele Identifier: CA16027691

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174202G>C (hg19) ; chr5:g.112838505G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838505G>C , CM000667.2:g.112838505G>C	GRCh38
NC_000005.9:g.112174202G>C , CM000667.1:g.112174202G>C	GRCh37
NC_000005.8:g.112202101G>C	NCBI36
NG_008481.4:g.150985G>C , LRG_130:g.150985G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.2576G>C	ENSP00000484935.2:n.2576G>C
ENST00000504915.3:c.2965G>C	ENSP00000473355.2:p.Asp989His
ENST00000505350.2:c.*2917G>C	ENSP00000481752.1:n.*2917G>C
ENST00000507379.6:c.2857G>C	ENSP00000423224.2:p.Asp953His
ENST00000509732.6:c.2911G>C	ENSP00000426541.2:p.Asp971His
ENST00000512211.7:c.2911G>C	ENSP00000423828.3:p.Asp971His
ENST00000257430.9:c.2911G>C MANE Select	ENSP00000257430.4:p.Asp971His
ENST00000257430.8:c.2911G>C	ENSP00000257430.4:p.Asp971His
ENST00000502371.2:c.1264G>C
ENST00000507379.5:c.2857G>C	ENSP00000423224.1:p.Asp953His
ENST00000508376.6:c.2911G>C	ENSP00000427089.2:p.Asp971His
ENST00000508624.5:c.*2233G>C	ENSP00000424265.1:n.*2233G>C
ENST00000512211.6:c.2911G>C	ENSP00000423828.2:p.Asp971His
ENST00000520401.1:c.230+9533G>C
NM_000038.5:c.2911G>C	NP_000029.2:p.Asp971His
NM_001127510.2:c.2911G>C	NP_001120982.1:p.Asp971His
NM_001127511.2:c.2857G>C	NP_001120983.2:p.Asp953His
NM_001354895.1:c.2911G>C	NP_001341824.1:p.Asp971His
NM_001354896.1:c.2965G>C	NP_001341825.1:p.Asp989His
NM_001354897.1:c.2941G>C	NP_001341826.1:p.Asp981His
NM_001354898.1:c.2836G>C	NP_001341827.1:p.Asp946His
NM_001354899.1:c.2827G>C	NP_001341828.1:p.Asp943His
NM_001354900.1:c.2788G>C	NP_001341829.1:p.Asp930His
NM_001354901.1:c.2734G>C	NP_001341830.1:p.Asp912His
NM_001354902.1:c.2638G>C	NP_001341831.1:p.Asp880His
NM_001354903.1:c.2608G>C	NP_001341832.1:p.Asp870His
NM_001354904.1:c.2533G>C	NP_001341833.1:p.Asp845His
NM_001354905.1:c.2431G>C	NP_001341834.1:p.Asp811His
NM_001354906.1:c.2062G>C	NP_001341835.1:p.Asp688His
NM_000038.6:c.2911G>C MANE Select	NP_000029.2:p.Asp971His
NM_001127510.3:c.2911G>C	NP_001120982.1:p.Asp971His
NM_001127511.3:c.2857G>C	NP_001120983.2:p.Asp953His
NM_001354895.2:c.2911G>C	NP_001341824.1:p.Asp971His
NM_001354896.2:c.2965G>C	NP_001341825.1:p.Asp989His
NM_001354897.2:c.2941G>C	NP_001341826.1:p.Asp981His
NM_001354898.2:c.2836G>C	NP_001341827.1:p.Asp946His
NM_001354899.2:c.2827G>C	NP_001341828.1:p.Asp943His
NM_001354900.2:c.2788G>C	NP_001341829.1:p.Asp930His
NM_001354901.2:c.2734G>C	NP_001341830.1:p.Asp912His
NM_001354902.2:c.2638G>C	NP_001341831.1:p.Asp880His
NM_001354903.2:c.2608G>C	NP_001341832.1:p.Asp870His
NM_001354904.2:c.2533G>C	NP_001341833.1:p.Asp845His
NM_001354905.2:c.2431G>C	NP_001341834.1:p.Asp811His
NM_001354906.2:c.2062G>C	NP_001341835.1:p.Asp688His