Canonical Allele Identifier: CA16028669

Gene: APC

Linked Data

• dbSNP Id: rs2149890117
• MyVariant Identifiers: chr5:g.112174640T>A (hg19) ; chr5:g.112838943T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838943T>A , CM000667.2:g.112838943T>A	GRCh38
NC_000005.9:g.112174640T>A , CM000667.1:g.112174640T>A	GRCh37
NC_000005.8:g.112202539T>A	NCBI36
NG_008481.4:g.151423T>A , LRG_130:g.151423T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3014T>A	ENSP00000484935.2:n.3014T>A
ENST00000504915.3:c.3403T>A	ENSP00000473355.2:p.Ser1135Thr
ENST00000505350.2:c.*3355T>A	ENSP00000481752.1:n.*3355T>A
ENST00000507379.6:c.3295T>A	ENSP00000423224.2:p.Ser1099Thr
ENST00000509732.6:c.3349T>A	ENSP00000426541.2:p.Ser1117Thr
ENST00000512211.7:c.3349T>A	ENSP00000423828.3:p.Ser1117Thr
ENST00000257430.9:c.3349T>A MANE Select	ENSP00000257430.4:p.Ser1117Thr
ENST00000257430.8:c.3349T>A	ENSP00000257430.4:p.Ser1117Thr
ENST00000502371.2:c.1702T>A
ENST00000507379.5:c.3295T>A	ENSP00000423224.1:p.Ser1099Thr
ENST00000508376.6:c.3349T>A	ENSP00000427089.2:p.Ser1117Thr
ENST00000508624.5:c.*2671T>A	ENSP00000424265.1:n.*2671T>A
ENST00000512211.6:c.3349T>A	ENSP00000423828.2:p.Ser1117Thr
ENST00000520401.1:c.230+9971T>A
NM_000038.5:c.3349T>A	NP_000029.2:p.Ser1117Thr
NM_001127510.2:c.3349T>A	NP_001120982.1:p.Ser1117Thr
NM_001127511.2:c.3295T>A	NP_001120983.2:p.Ser1099Thr
NM_001354895.1:c.3349T>A	NP_001341824.1:p.Ser1117Thr
NM_001354896.1:c.3403T>A	NP_001341825.1:p.Ser1135Thr
NM_001354897.1:c.3379T>A	NP_001341826.1:p.Ser1127Thr
NM_001354898.1:c.3274T>A	NP_001341827.1:p.Ser1092Thr
NM_001354899.1:c.3265T>A	NP_001341828.1:p.Ser1089Thr
NM_001354900.1:c.3226T>A	NP_001341829.1:p.Ser1076Thr
NM_001354901.1:c.3172T>A	NP_001341830.1:p.Ser1058Thr
NM_001354902.1:c.3076T>A	NP_001341831.1:p.Ser1026Thr
NM_001354903.1:c.3046T>A	NP_001341832.1:p.Ser1016Thr
NM_001354904.1:c.2971T>A	NP_001341833.1:p.Ser991Thr
NM_001354905.1:c.2869T>A	NP_001341834.1:p.Ser957Thr
NM_001354906.1:c.2500T>A	NP_001341835.1:p.Ser834Thr
NM_000038.6:c.3349T>A MANE Select	NP_000029.2:p.Ser1117Thr
NM_001127510.3:c.3349T>A	NP_001120982.1:p.Ser1117Thr
NM_001127511.3:c.3295T>A	NP_001120983.2:p.Ser1099Thr
NM_001354895.2:c.3349T>A	NP_001341824.1:p.Ser1117Thr
NM_001354896.2:c.3403T>A	NP_001341825.1:p.Ser1135Thr
NM_001354897.2:c.3379T>A	NP_001341826.1:p.Ser1127Thr
NM_001354898.2:c.3274T>A	NP_001341827.1:p.Ser1092Thr
NM_001354899.2:c.3265T>A	NP_001341828.1:p.Ser1089Thr
NM_001354900.2:c.3226T>A	NP_001341829.1:p.Ser1076Thr
NM_001354901.2:c.3172T>A	NP_001341830.1:p.Ser1058Thr
NM_001354902.2:c.3076T>A	NP_001341831.1:p.Ser1026Thr
NM_001354903.2:c.3046T>A	NP_001341832.1:p.Ser1016Thr
NM_001354904.2:c.2971T>A	NP_001341833.1:p.Ser991Thr
NM_001354905.2:c.2869T>A	NP_001341834.1:p.Ser957Thr
NM_001354906.2:c.2500T>A	NP_001341835.1:p.Ser834Thr