Canonical Allele Identifier: CA16028147

Gene: APC

Linked Data

• dbSNP Id: rs1291598405
• MyVariant Identifiers: chr5:g.112174401A>C (hg19) ; chr5:g.112838704A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838704A>C , CM000667.2:g.112838704A>C	GRCh38
NC_000005.9:g.112174401A>C , CM000667.1:g.112174401A>C	GRCh37
NC_000005.8:g.112202300A>C	NCBI36
NG_008481.4:g.151184A>C , LRG_130:g.151184A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2775A>C	ENSP00000484935.2:n.2775A>C
ENST00000504915.3:c.3164A>C	ENSP00000473355.2:p.Asn1055Thr
ENST00000505350.2:c.*3116A>C	ENSP00000481752.1:n.*3116A>C
ENST00000507379.6:c.3056A>C	ENSP00000423224.2:p.Asn1019Thr
ENST00000509732.6:c.3110A>C	ENSP00000426541.2:p.Asn1037Thr
ENST00000512211.7:c.3110A>C	ENSP00000423828.3:p.Asn1037Thr
ENST00000257430.9:c.3110A>C MANE Select	ENSP00000257430.4:p.Asn1037Thr
ENST00000257430.8:c.3110A>C	ENSP00000257430.4:p.Asn1037Thr
ENST00000502371.2:c.1463A>C
ENST00000507379.5:c.3056A>C	ENSP00000423224.1:p.Asn1019Thr
ENST00000508376.6:c.3110A>C	ENSP00000427089.2:p.Asn1037Thr
ENST00000508624.5:c.*2432A>C	ENSP00000424265.1:n.*2432A>C
ENST00000512211.6:c.3110A>C	ENSP00000423828.2:p.Asn1037Thr
ENST00000520401.1:c.230+9732A>C
NM_000038.5:c.3110A>C	NP_000029.2:p.Asn1037Thr
NM_001127510.2:c.3110A>C	NP_001120982.1:p.Asn1037Thr
NM_001127511.2:c.3056A>C	NP_001120983.2:p.Asn1019Thr
NM_001354895.1:c.3110A>C	NP_001341824.1:p.Asn1037Thr
NM_001354896.1:c.3164A>C	NP_001341825.1:p.Asn1055Thr
NM_001354897.1:c.3140A>C	NP_001341826.1:p.Asn1047Thr
NM_001354898.1:c.3035A>C	NP_001341827.1:p.Asn1012Thr
NM_001354899.1:c.3026A>C	NP_001341828.1:p.Asn1009Thr
NM_001354900.1:c.2987A>C	NP_001341829.1:p.Asn996Thr
NM_001354901.1:c.2933A>C	NP_001341830.1:p.Asn978Thr
NM_001354902.1:c.2837A>C	NP_001341831.1:p.Asn946Thr
NM_001354903.1:c.2807A>C	NP_001341832.1:p.Asn936Thr
NM_001354904.1:c.2732A>C	NP_001341833.1:p.Asn911Thr
NM_001354905.1:c.2630A>C	NP_001341834.1:p.Asn877Thr
NM_001354906.1:c.2261A>C	NP_001341835.1:p.Asn754Thr
NM_000038.6:c.3110A>C MANE Select	NP_000029.2:p.Asn1037Thr
NM_001127510.3:c.3110A>C	NP_001120982.1:p.Asn1037Thr
NM_001127511.3:c.3056A>C	NP_001120983.2:p.Asn1019Thr
NM_001354895.2:c.3110A>C	NP_001341824.1:p.Asn1037Thr
NM_001354896.2:c.3164A>C	NP_001341825.1:p.Asn1055Thr
NM_001354897.2:c.3140A>C	NP_001341826.1:p.Asn1047Thr
NM_001354898.2:c.3035A>C	NP_001341827.1:p.Asn1012Thr
NM_001354899.2:c.3026A>C	NP_001341828.1:p.Asn1009Thr
NM_001354900.2:c.2987A>C	NP_001341829.1:p.Asn996Thr
NM_001354901.2:c.2933A>C	NP_001341830.1:p.Asn978Thr
NM_001354902.2:c.2837A>C	NP_001341831.1:p.Asn946Thr
NM_001354903.2:c.2807A>C	NP_001341832.1:p.Asn936Thr
NM_001354904.2:c.2732A>C	NP_001341833.1:p.Asn911Thr
NM_001354905.2:c.2630A>C	NP_001341834.1:p.Asn877Thr
NM_001354906.2:c.2261A>C	NP_001341835.1:p.Asn754Thr