Canonical Allele Identifier: CA16038997

Gene: APC

Linked Data

• dbSNP Id: rs2149999723
• MyVariant Identifiers: chr5:g.112179423T>G (hg19) ; chr5:g.112843726T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843726T>G , CM000667.2:g.112843726T>G	GRCh38
NC_000005.9:g.112179423T>G , CM000667.1:g.112179423T>G	GRCh37
NC_000005.8:g.112207322T>G	NCBI36
NG_008481.4:g.156206T>G , LRG_130:g.156206T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.8186T>G	ENSP00000473355.2:p.Val2729Gly
ENST00000505350.2:c.*8138T>G	ENSP00000481752.1:n.*8138T>G
ENST00000507379.6:c.8078T>G	ENSP00000423224.2:p.Val2693Gly
ENST00000509732.6:c.8132T>G	ENSP00000426541.2:p.Val2711Gly
ENST00000512211.7:c.8132T>G	ENSP00000423828.3:p.Val2711Gly
ENST00000257430.9:c.8132T>G MANE Select	ENSP00000257430.4:p.Val2711Gly
ENST00000257430.8:c.8132T>G	ENSP00000257430.4:p.Val2711Gly
ENST00000508376.6:c.8132T>G	ENSP00000427089.2:p.Val2711Gly
ENST00000520401.1:c.231-12923T>G
NM_000038.5:c.8132T>G	NP_000029.2:p.Val2711Gly
NM_001127510.2:c.8132T>G	NP_001120982.1:p.Val2711Gly
NM_001127511.2:c.8078T>G	NP_001120983.2:p.Val2693Gly
NM_001354895.1:c.8132T>G	NP_001341824.1:p.Val2711Gly
NM_001354896.1:c.8186T>G	NP_001341825.1:p.Val2729Gly
NM_001354897.1:c.8162T>G	NP_001341826.1:p.Val2721Gly
NM_001354898.1:c.8057T>G	NP_001341827.1:p.Val2686Gly
NM_001354899.1:c.8048T>G	NP_001341828.1:p.Val2683Gly
NM_001354900.1:c.8009T>G	NP_001341829.1:p.Val2670Gly
NM_001354901.1:c.7955T>G	NP_001341830.1:p.Val2652Gly
NM_001354902.1:c.7859T>G	NP_001341831.1:p.Val2620Gly
NM_001354903.1:c.7829T>G	NP_001341832.1:p.Val2610Gly
NM_001354904.1:c.7754T>G	NP_001341833.1:p.Val2585Gly
NM_001354905.1:c.7652T>G	NP_001341834.1:p.Val2551Gly
NM_001354906.1:c.7283T>G	NP_001341835.1:p.Val2428Gly
NM_000038.6:c.8132T>G MANE Select	NP_000029.2:p.Val2711Gly
NM_001127510.3:c.8132T>G	NP_001120982.1:p.Val2711Gly
NM_001127511.3:c.8078T>G	NP_001120983.2:p.Val2693Gly
NM_001354895.2:c.8132T>G	NP_001341824.1:p.Val2711Gly
NM_001354896.2:c.8186T>G	NP_001341825.1:p.Val2729Gly
NM_001354897.2:c.8162T>G	NP_001341826.1:p.Val2721Gly
NM_001354898.2:c.8057T>G	NP_001341827.1:p.Val2686Gly
NM_001354899.2:c.8048T>G	NP_001341828.1:p.Val2683Gly
NM_001354900.2:c.8009T>G	NP_001341829.1:p.Val2670Gly
NM_001354901.2:c.7955T>G	NP_001341830.1:p.Val2652Gly
NM_001354902.2:c.7859T>G	NP_001341831.1:p.Val2620Gly
NM_001354903.2:c.7829T>G	NP_001341832.1:p.Val2610Gly
NM_001354904.2:c.7754T>G	NP_001341833.1:p.Val2585Gly
NM_001354905.2:c.7652T>G	NP_001341834.1:p.Val2551Gly
NM_001354906.2:c.7283T>G	NP_001341835.1:p.Val2428Gly