Canonical Allele Identifier: CA10578446

Gene: APC

Linked Data

• ClinVar Variation Id: 231400
• ClinVar RCV Id: RCV000214071 ; RCV003534517
• dbSNP Id: rs876659135
• gnomAD v2: 5-112178820-A-G
• gnomAD v3: 5-112843123-A-G
• gnomAD v4: 5-112843123-A-G
• MyVariant Identifiers: chr5:g.112178820A>G (hg19) ; chr5:g.112843123A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843123A>G , CM000667.2:g.112843123A>G	GRCh38
NC_000005.9:g.112178820A>G , CM000667.1:g.112178820A>G	GRCh37
NC_000005.8:g.112206719A>G	NCBI36
NG_008481.4:g.155603A>G , LRG_130:g.155603A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7583A>G	ENSP00000473355.2:p.Asn2528Ser
ENST00000505350.2:c.*7535A>G	ENSP00000481752.1:n.*7535A>G
ENST00000507379.6:c.7475A>G	ENSP00000423224.2:p.Asn2492Ser
ENST00000509732.6:c.7529A>G	ENSP00000426541.2:p.Asn2510Ser
ENST00000512211.7:c.7529A>G	ENSP00000423828.3:p.Asn2510Ser
ENST00000257430.9:c.7529A>G MANE Select	ENSP00000257430.4:p.Asn2510Ser
ENST00000257430.8:c.7529A>G	ENSP00000257430.4:p.Asn2510Ser
ENST00000508376.6:c.7529A>G	ENSP00000427089.2:p.Asn2510Ser
ENST00000520401.1:c.231-13526A>G
NM_000038.5:c.7529A>G	NP_000029.2:p.Asn2510Ser
NM_001127510.2:c.7529A>G	NP_001120982.1:p.Asn2510Ser
NM_001127511.2:c.7475A>G	NP_001120983.2:p.Asn2492Ser
NM_001354895.1:c.7529A>G	NP_001341824.1:p.Asn2510Ser
NM_001354896.1:c.7583A>G	NP_001341825.1:p.Asn2528Ser
NM_001354897.1:c.7559A>G	NP_001341826.1:p.Asn2520Ser
NM_001354898.1:c.7454A>G	NP_001341827.1:p.Asn2485Ser
NM_001354899.1:c.7445A>G	NP_001341828.1:p.Asn2482Ser
NM_001354900.1:c.7406A>G	NP_001341829.1:p.Asn2469Ser
NM_001354901.1:c.7352A>G	NP_001341830.1:p.Asn2451Ser
NM_001354902.1:c.7256A>G	NP_001341831.1:p.Asn2419Ser
NM_001354903.1:c.7226A>G	NP_001341832.1:p.Asn2409Ser
NM_001354904.1:c.7151A>G	NP_001341833.1:p.Asn2384Ser
NM_001354905.1:c.7049A>G	NP_001341834.1:p.Asn2350Ser
NM_001354906.1:c.6680A>G	NP_001341835.1:p.Asn2227Ser
NM_000038.6:c.7529A>G MANE Select	NP_000029.2:p.Asn2510Ser
NM_001127510.3:c.7529A>G	NP_001120982.1:p.Asn2510Ser
NM_001127511.3:c.7475A>G	NP_001120983.2:p.Asn2492Ser
NM_001354895.2:c.7529A>G	NP_001341824.1:p.Asn2510Ser
NM_001354896.2:c.7583A>G	NP_001341825.1:p.Asn2528Ser
NM_001354897.2:c.7559A>G	NP_001341826.1:p.Asn2520Ser
NM_001354898.2:c.7454A>G	NP_001341827.1:p.Asn2485Ser
NM_001354899.2:c.7445A>G	NP_001341828.1:p.Asn2482Ser
NM_001354900.2:c.7406A>G	NP_001341829.1:p.Asn2469Ser
NM_001354901.2:c.7352A>G	NP_001341830.1:p.Asn2451Ser
NM_001354902.2:c.7256A>G	NP_001341831.1:p.Asn2419Ser
NM_001354903.2:c.7226A>G	NP_001341832.1:p.Asn2409Ser
NM_001354904.2:c.7151A>G	NP_001341833.1:p.Asn2384Ser
NM_001354905.2:c.7049A>G	NP_001341834.1:p.Asn2350Ser
NM_001354906.2:c.6680A>G	NP_001341835.1:p.Asn2227Ser