Canonical Allele Identifier: CA16027709

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174210T>A (hg19) ; chr5:g.112838513T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838513T>A , CM000667.2:g.112838513T>A	GRCh38
NC_000005.9:g.112174210T>A , CM000667.1:g.112174210T>A	GRCh37
NC_000005.8:g.112202109T>A	NCBI36
NG_008481.4:g.150993T>A , LRG_130:g.150993T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.2584T>A	ENSP00000484935.2:n.2584T>A
ENST00000504915.3:c.2973T>A	ENSP00000473355.2:p.Tyr991Ter
ENST00000505350.2:c.*2925T>A	ENSP00000481752.1:n.*2925T>A
ENST00000507379.6:c.2865T>A	ENSP00000423224.2:p.Tyr955Ter
ENST00000509732.6:c.2919T>A	ENSP00000426541.2:p.Tyr973Ter
ENST00000512211.7:c.2919T>A	ENSP00000423828.3:p.Tyr973Ter
ENST00000257430.9:c.2919T>A MANE Select	ENSP00000257430.4:p.Tyr973Ter
ENST00000257430.8:c.2919T>A	ENSP00000257430.4:p.Tyr973Ter
ENST00000502371.2:c.1272T>A
ENST00000507379.5:c.2865T>A	ENSP00000423224.1:p.Tyr955Ter
ENST00000508376.6:c.2919T>A	ENSP00000427089.2:p.Tyr973Ter
ENST00000508624.5:c.*2241T>A	ENSP00000424265.1:n.*2241T>A
ENST00000512211.6:c.2919T>A	ENSP00000423828.2:p.Tyr973Ter
ENST00000520401.1:c.230+9541T>A
NM_000038.5:c.2919T>A	NP_000029.2:p.Tyr973Ter
NM_001127510.2:c.2919T>A	NP_001120982.1:p.Tyr973Ter
NM_001127511.2:c.2865T>A	NP_001120983.2:p.Tyr955Ter
NM_001354895.1:c.2919T>A	NP_001341824.1:p.Tyr973Ter
NM_001354896.1:c.2973T>A	NP_001341825.1:p.Tyr991Ter
NM_001354897.1:c.2949T>A	NP_001341826.1:p.Tyr983Ter
NM_001354898.1:c.2844T>A	NP_001341827.1:p.Tyr948Ter
NM_001354899.1:c.2835T>A	NP_001341828.1:p.Tyr945Ter
NM_001354900.1:c.2796T>A	NP_001341829.1:p.Tyr932Ter
NM_001354901.1:c.2742T>A	NP_001341830.1:p.Tyr914Ter
NM_001354902.1:c.2646T>A	NP_001341831.1:p.Tyr882Ter
NM_001354903.1:c.2616T>A	NP_001341832.1:p.Tyr872Ter
NM_001354904.1:c.2541T>A	NP_001341833.1:p.Tyr847Ter
NM_001354905.1:c.2439T>A	NP_001341834.1:p.Tyr813Ter
NM_001354906.1:c.2070T>A	NP_001341835.1:p.Tyr690Ter
NM_000038.6:c.2919T>A MANE Select	NP_000029.2:p.Tyr973Ter
NM_001127510.3:c.2919T>A	NP_001120982.1:p.Tyr973Ter
NM_001127511.3:c.2865T>A	NP_001120983.2:p.Tyr955Ter
NM_001354895.2:c.2919T>A	NP_001341824.1:p.Tyr973Ter
NM_001354896.2:c.2973T>A	NP_001341825.1:p.Tyr991Ter
NM_001354897.2:c.2949T>A	NP_001341826.1:p.Tyr983Ter
NM_001354898.2:c.2844T>A	NP_001341827.1:p.Tyr948Ter
NM_001354899.2:c.2835T>A	NP_001341828.1:p.Tyr945Ter
NM_001354900.2:c.2796T>A	NP_001341829.1:p.Tyr932Ter
NM_001354901.2:c.2742T>A	NP_001341830.1:p.Tyr914Ter
NM_001354902.2:c.2646T>A	NP_001341831.1:p.Tyr882Ter
NM_001354903.2:c.2616T>A	NP_001341832.1:p.Tyr872Ter
NM_001354904.2:c.2541T>A	NP_001341833.1:p.Tyr847Ter
NM_001354905.2:c.2439T>A	NP_001341834.1:p.Tyr813Ter
NM_001354906.2:c.2070T>A	NP_001341835.1:p.Tyr690Ter