Canonical Allele Identifier: CA16028151

Gene: APC

Linked Data

• ClinVar Variation Id: 2452689
• ClinVar RCV Id: RCV003177463
• dbSNP Id: rs1580631002
• MyVariant Identifiers: chr5:g.112174402C>G (hg19) ; chr5:g.112838705C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838705C>G , CM000667.2:g.112838705C>G	GRCh38
NC_000005.9:g.112174402C>G , CM000667.1:g.112174402C>G	GRCh37
NC_000005.8:g.112202301C>G	NCBI36
NG_008481.4:g.151185C>G , LRG_130:g.151185C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2776C>G	ENSP00000484935.2:n.2776C>G
ENST00000504915.3:c.3165C>G	ENSP00000473355.2:p.Asn1055Lys
ENST00000505350.2:c.*3117C>G	ENSP00000481752.1:n.*3117C>G
ENST00000507379.6:c.3057C>G	ENSP00000423224.2:p.Asn1019Lys
ENST00000509732.6:c.3111C>G	ENSP00000426541.2:p.Asn1037Lys
ENST00000512211.7:c.3111C>G	ENSP00000423828.3:p.Asn1037Lys
ENST00000257430.9:c.3111C>G MANE Select	ENSP00000257430.4:p.Asn1037Lys
ENST00000257430.8:c.3111C>G	ENSP00000257430.4:p.Asn1037Lys
ENST00000502371.2:c.1464C>G
ENST00000507379.5:c.3057C>G	ENSP00000423224.1:p.Asn1019Lys
ENST00000508376.6:c.3111C>G	ENSP00000427089.2:p.Asn1037Lys
ENST00000508624.5:c.*2433C>G	ENSP00000424265.1:n.*2433C>G
ENST00000512211.6:c.3111C>G	ENSP00000423828.2:p.Asn1037Lys
ENST00000520401.1:c.230+9733C>G
NM_000038.5:c.3111C>G	NP_000029.2:p.Asn1037Lys
NM_001127510.2:c.3111C>G	NP_001120982.1:p.Asn1037Lys
NM_001127511.2:c.3057C>G	NP_001120983.2:p.Asn1019Lys
NM_001354895.1:c.3111C>G	NP_001341824.1:p.Asn1037Lys
NM_001354896.1:c.3165C>G	NP_001341825.1:p.Asn1055Lys
NM_001354897.1:c.3141C>G	NP_001341826.1:p.Asn1047Lys
NM_001354898.1:c.3036C>G	NP_001341827.1:p.Asn1012Lys
NM_001354899.1:c.3027C>G	NP_001341828.1:p.Asn1009Lys
NM_001354900.1:c.2988C>G	NP_001341829.1:p.Asn996Lys
NM_001354901.1:c.2934C>G	NP_001341830.1:p.Asn978Lys
NM_001354902.1:c.2838C>G	NP_001341831.1:p.Asn946Lys
NM_001354903.1:c.2808C>G	NP_001341832.1:p.Asn936Lys
NM_001354904.1:c.2733C>G	NP_001341833.1:p.Asn911Lys
NM_001354905.1:c.2631C>G	NP_001341834.1:p.Asn877Lys
NM_001354906.1:c.2262C>G	NP_001341835.1:p.Asn754Lys
NM_000038.6:c.3111C>G MANE Select	NP_000029.2:p.Asn1037Lys
NM_001127510.3:c.3111C>G	NP_001120982.1:p.Asn1037Lys
NM_001127511.3:c.3057C>G	NP_001120983.2:p.Asn1019Lys
NM_001354895.2:c.3111C>G	NP_001341824.1:p.Asn1037Lys
NM_001354896.2:c.3165C>G	NP_001341825.1:p.Asn1055Lys
NM_001354897.2:c.3141C>G	NP_001341826.1:p.Asn1047Lys
NM_001354898.2:c.3036C>G	NP_001341827.1:p.Asn1012Lys
NM_001354899.2:c.3027C>G	NP_001341828.1:p.Asn1009Lys
NM_001354900.2:c.2988C>G	NP_001341829.1:p.Asn996Lys
NM_001354901.2:c.2934C>G	NP_001341830.1:p.Asn978Lys
NM_001354902.2:c.2838C>G	NP_001341831.1:p.Asn946Lys
NM_001354903.2:c.2808C>G	NP_001341832.1:p.Asn936Lys
NM_001354904.2:c.2733C>G	NP_001341833.1:p.Asn911Lys
NM_001354905.2:c.2631C>G	NP_001341834.1:p.Asn877Lys
NM_001354906.2:c.2262C>G	NP_001341835.1:p.Asn754Lys