Canonical Allele Identifier: CA16037957

Gene: APC

Linked Data

• dbSNP Id: rs1248219316
• MyVariant Identifiers: chr5:g.112178944C>G (hg19) ; chr5:g.112843247C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843247C>G , CM000667.2:g.112843247C>G	GRCh38
NC_000005.9:g.112178944C>G , CM000667.1:g.112178944C>G	GRCh37
NC_000005.8:g.112206843C>G	NCBI36
NG_008481.4:g.155727C>G , LRG_130:g.155727C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7707C>G	ENSP00000473355.2:p.His2569Gln
ENST00000505350.2:c.*7659C>G	ENSP00000481752.1:n.*7659C>G
ENST00000507379.6:c.7599C>G	ENSP00000423224.2:p.His2533Gln
ENST00000509732.6:c.7653C>G	ENSP00000426541.2:p.His2551Gln
ENST00000512211.7:c.7653C>G	ENSP00000423828.3:p.His2551Gln
ENST00000257430.9:c.7653C>G MANE Select	ENSP00000257430.4:p.His2551Gln
ENST00000257430.8:c.7653C>G	ENSP00000257430.4:p.His2551Gln
ENST00000508376.6:c.7653C>G	ENSP00000427089.2:p.His2551Gln
ENST00000520401.1:c.231-13402C>G
NM_000038.5:c.7653C>G	NP_000029.2:p.His2551Gln
NM_001127510.2:c.7653C>G	NP_001120982.1:p.His2551Gln
NM_001127511.2:c.7599C>G	NP_001120983.2:p.His2533Gln
NM_001354895.1:c.7653C>G	NP_001341824.1:p.His2551Gln
NM_001354896.1:c.7707C>G	NP_001341825.1:p.His2569Gln
NM_001354897.1:c.7683C>G	NP_001341826.1:p.His2561Gln
NM_001354898.1:c.7578C>G	NP_001341827.1:p.His2526Gln
NM_001354899.1:c.7569C>G	NP_001341828.1:p.His2523Gln
NM_001354900.1:c.7530C>G	NP_001341829.1:p.His2510Gln
NM_001354901.1:c.7476C>G	NP_001341830.1:p.His2492Gln
NM_001354902.1:c.7380C>G	NP_001341831.1:p.His2460Gln
NM_001354903.1:c.7350C>G	NP_001341832.1:p.His2450Gln
NM_001354904.1:c.7275C>G	NP_001341833.1:p.His2425Gln
NM_001354905.1:c.7173C>G	NP_001341834.1:p.His2391Gln
NM_001354906.1:c.6804C>G	NP_001341835.1:p.His2268Gln
NM_000038.6:c.7653C>G MANE Select	NP_000029.2:p.His2551Gln
NM_001127510.3:c.7653C>G	NP_001120982.1:p.His2551Gln
NM_001127511.3:c.7599C>G	NP_001120983.2:p.His2533Gln
NM_001354895.2:c.7653C>G	NP_001341824.1:p.His2551Gln
NM_001354896.2:c.7707C>G	NP_001341825.1:p.His2569Gln
NM_001354897.2:c.7683C>G	NP_001341826.1:p.His2561Gln
NM_001354898.2:c.7578C>G	NP_001341827.1:p.His2526Gln
NM_001354899.2:c.7569C>G	NP_001341828.1:p.His2523Gln
NM_001354900.2:c.7530C>G	NP_001341829.1:p.His2510Gln
NM_001354901.2:c.7476C>G	NP_001341830.1:p.His2492Gln
NM_001354902.2:c.7380C>G	NP_001341831.1:p.His2460Gln
NM_001354903.2:c.7350C>G	NP_001341832.1:p.His2450Gln
NM_001354904.2:c.7275C>G	NP_001341833.1:p.His2425Gln
NM_001354905.2:c.7173C>G	NP_001341834.1:p.His2391Gln
NM_001354906.2:c.6804C>G	NP_001341835.1:p.His2268Gln