Canonical Allele Identifier: CA16027702

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174206G>T (hg19) ; chr5:g.112838509G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838509G>T , CM000667.2:g.112838509G>T	GRCh38
NC_000005.9:g.112174206G>T , CM000667.1:g.112174206G>T	GRCh37
NC_000005.8:g.112202105G>T	NCBI36
NG_008481.4:g.150989G>T , LRG_130:g.150989G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.2580G>T	ENSP00000484935.2:n.2580G>T
ENST00000504915.3:c.2969G>T	ENSP00000473355.2:p.Gly990Val
ENST00000505350.2:c.*2921G>T	ENSP00000481752.1:n.*2921G>T
ENST00000507379.6:c.2861G>T	ENSP00000423224.2:p.Gly954Val
ENST00000509732.6:c.2915G>T	ENSP00000426541.2:p.Gly972Val
ENST00000512211.7:c.2915G>T	ENSP00000423828.3:p.Gly972Val
ENST00000257430.9:c.2915G>T MANE Select	ENSP00000257430.4:p.Gly972Val
ENST00000257430.8:c.2915G>T	ENSP00000257430.4:p.Gly972Val
ENST00000502371.2:c.1268G>T
ENST00000507379.5:c.2861G>T	ENSP00000423224.1:p.Gly954Val
ENST00000508376.6:c.2915G>T	ENSP00000427089.2:p.Gly972Val
ENST00000508624.5:c.*2237G>T	ENSP00000424265.1:n.*2237G>T
ENST00000512211.6:c.2915G>T	ENSP00000423828.2:p.Gly972Val
ENST00000520401.1:c.230+9537G>T
NM_000038.5:c.2915G>T	NP_000029.2:p.Gly972Val
NM_001127510.2:c.2915G>T	NP_001120982.1:p.Gly972Val
NM_001127511.2:c.2861G>T	NP_001120983.2:p.Gly954Val
NM_001354895.1:c.2915G>T	NP_001341824.1:p.Gly972Val
NM_001354896.1:c.2969G>T	NP_001341825.1:p.Gly990Val
NM_001354897.1:c.2945G>T	NP_001341826.1:p.Gly982Val
NM_001354898.1:c.2840G>T	NP_001341827.1:p.Gly947Val
NM_001354899.1:c.2831G>T	NP_001341828.1:p.Gly944Val
NM_001354900.1:c.2792G>T	NP_001341829.1:p.Gly931Val
NM_001354901.1:c.2738G>T	NP_001341830.1:p.Gly913Val
NM_001354902.1:c.2642G>T	NP_001341831.1:p.Gly881Val
NM_001354903.1:c.2612G>T	NP_001341832.1:p.Gly871Val
NM_001354904.1:c.2537G>T	NP_001341833.1:p.Gly846Val
NM_001354905.1:c.2435G>T	NP_001341834.1:p.Gly812Val
NM_001354906.1:c.2066G>T	NP_001341835.1:p.Gly689Val
NM_000038.6:c.2915G>T MANE Select	NP_000029.2:p.Gly972Val
NM_001127510.3:c.2915G>T	NP_001120982.1:p.Gly972Val
NM_001127511.3:c.2861G>T	NP_001120983.2:p.Gly954Val
NM_001354895.2:c.2915G>T	NP_001341824.1:p.Gly972Val
NM_001354896.2:c.2969G>T	NP_001341825.1:p.Gly990Val
NM_001354897.2:c.2945G>T	NP_001341826.1:p.Gly982Val
NM_001354898.2:c.2840G>T	NP_001341827.1:p.Gly947Val
NM_001354899.2:c.2831G>T	NP_001341828.1:p.Gly944Val
NM_001354900.2:c.2792G>T	NP_001341829.1:p.Gly931Val
NM_001354901.2:c.2738G>T	NP_001341830.1:p.Gly913Val
NM_001354902.2:c.2642G>T	NP_001341831.1:p.Gly881Val
NM_001354903.2:c.2612G>T	NP_001341832.1:p.Gly871Val
NM_001354904.2:c.2537G>T	NP_001341833.1:p.Gly846Val
NM_001354905.2:c.2435G>T	NP_001341834.1:p.Gly812Val
NM_001354906.2:c.2066G>T	NP_001341835.1:p.Gly689Val