Canonical Allele Identifier: CA16038404

Gene: APC

Linked Data

• dbSNP Id: rs876659239
• MyVariant Identifiers: chr5:g.112179147A>T (hg19) ; chr5:g.112843450A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843450A>T , CM000667.2:g.112843450A>T	GRCh38
NC_000005.9:g.112179147A>T , CM000667.1:g.112179147A>T	GRCh37
NC_000005.8:g.112207046A>T	NCBI36
NG_008481.4:g.155930A>T , LRG_130:g.155930A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7910A>T	ENSP00000473355.2:p.Glu2637Val
ENST00000505350.2:c.*7862A>T	ENSP00000481752.1:n.*7862A>T
ENST00000507379.6:c.7802A>T	ENSP00000423224.2:p.Glu2601Val
ENST00000509732.6:c.7856A>T	ENSP00000426541.2:p.Glu2619Val
ENST00000512211.7:c.7856A>T	ENSP00000423828.3:p.Glu2619Val
ENST00000257430.9:c.7856A>T MANE Select	ENSP00000257430.4:p.Glu2619Val
ENST00000257430.8:c.7856A>T	ENSP00000257430.4:p.Glu2619Val
ENST00000508376.6:c.7856A>T	ENSP00000427089.2:p.Glu2619Val
ENST00000520401.1:c.231-13199A>T
NM_000038.5:c.7856A>T	NP_000029.2:p.Glu2619Val
NM_001127510.2:c.7856A>T	NP_001120982.1:p.Glu2619Val
NM_001127511.2:c.7802A>T	NP_001120983.2:p.Glu2601Val
NM_001354895.1:c.7856A>T	NP_001341824.1:p.Glu2619Val
NM_001354896.1:c.7910A>T	NP_001341825.1:p.Glu2637Val
NM_001354897.1:c.7886A>T	NP_001341826.1:p.Glu2629Val
NM_001354898.1:c.7781A>T	NP_001341827.1:p.Glu2594Val
NM_001354899.1:c.7772A>T	NP_001341828.1:p.Glu2591Val
NM_001354900.1:c.7733A>T	NP_001341829.1:p.Glu2578Val
NM_001354901.1:c.7679A>T	NP_001341830.1:p.Glu2560Val
NM_001354902.1:c.7583A>T	NP_001341831.1:p.Glu2528Val
NM_001354903.1:c.7553A>T	NP_001341832.1:p.Glu2518Val
NM_001354904.1:c.7478A>T	NP_001341833.1:p.Glu2493Val
NM_001354905.1:c.7376A>T	NP_001341834.1:p.Glu2459Val
NM_001354906.1:c.7007A>T	NP_001341835.1:p.Glu2336Val
NM_000038.6:c.7856A>T MANE Select	NP_000029.2:p.Glu2619Val
NM_001127510.3:c.7856A>T	NP_001120982.1:p.Glu2619Val
NM_001127511.3:c.7802A>T	NP_001120983.2:p.Glu2601Val
NM_001354895.2:c.7856A>T	NP_001341824.1:p.Glu2619Val
NM_001354896.2:c.7910A>T	NP_001341825.1:p.Glu2637Val
NM_001354897.2:c.7886A>T	NP_001341826.1:p.Glu2629Val
NM_001354898.2:c.7781A>T	NP_001341827.1:p.Glu2594Val
NM_001354899.2:c.7772A>T	NP_001341828.1:p.Glu2591Val
NM_001354900.2:c.7733A>T	NP_001341829.1:p.Glu2578Val
NM_001354901.2:c.7679A>T	NP_001341830.1:p.Glu2560Val
NM_001354902.2:c.7583A>T	NP_001341831.1:p.Glu2528Val
NM_001354903.2:c.7553A>T	NP_001341832.1:p.Glu2518Val
NM_001354904.2:c.7478A>T	NP_001341833.1:p.Glu2493Val
NM_001354905.2:c.7376A>T	NP_001341834.1:p.Glu2459Val
NM_001354906.2:c.7007A>T	NP_001341835.1:p.Glu2336Val