Canonical Allele Identifier: CA009779

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840487T>C , CM000667.2:g.112840487T>C	GRCh38
NC_000005.9:g.112176184T>C , CM000667.1:g.112176184T>C	GRCh37
NC_000005.8:g.112204083T>C	NCBI36
NG_008481.4:g.152967T>C , LRG_130:g.152967T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.4893T>C MANE Select	NP_000029.2:p.Ser1631=
ENST00000257430.9:c.4893T>C MANE Select	ENSP00000257430.4:p.Ser1631=
NM_000038.5:c.4893T>C	NP_000029.2:p.Ser1631=
NM_001127510.2:c.4893T>C	NP_001120982.1:p.Ser1631=
NM_001127510.3:c.4893T>C	NP_001120982.1:p.Ser1631=
NM_001127511.2:c.4839T>C	NP_001120983.2:p.Ser1613=
NM_001127511.3:c.4839T>C	NP_001120983.2:p.Ser1613=
NM_001354895.1:c.4893T>C	NP_001341824.1:p.Ser1631=
NM_001354895.2:c.4893T>C	NP_001341824.1:p.Ser1631=
NM_001354896.1:c.4947T>C	NP_001341825.1:p.Ser1649=
NM_001354896.2:c.4947T>C	NP_001341825.1:p.Ser1649=
NM_001354897.1:c.4923T>C	NP_001341826.1:p.Ser1641=
NM_001354897.2:c.4923T>C	NP_001341826.1:p.Ser1641=
NM_001354898.1:c.4818T>C	NP_001341827.1:p.Ser1606=
NM_001354898.2:c.4818T>C	NP_001341827.1:p.Ser1606=
NM_001354899.1:c.4809T>C	NP_001341828.1:p.Ser1603=
NM_001354899.2:c.4809T>C	NP_001341828.1:p.Ser1603=
NM_001354900.1:c.4770T>C	NP_001341829.1:p.Ser1590=
NM_001354900.2:c.4770T>C	NP_001341829.1:p.Ser1590=
NM_001354901.1:c.4716T>C	NP_001341830.1:p.Ser1572=
NM_001354901.2:c.4716T>C	NP_001341830.1:p.Ser1572=
NM_001354902.1:c.4620T>C	NP_001341831.1:p.Ser1540=
NM_001354902.2:c.4620T>C	NP_001341831.1:p.Ser1540=
NM_001354903.1:c.4590T>C	NP_001341832.1:p.Ser1530=
NM_001354903.2:c.4590T>C	NP_001341832.1:p.Ser1530=
NM_001354904.1:c.4515T>C	NP_001341833.1:p.Ser1505=
NM_001354904.2:c.4515T>C	NP_001341833.1:p.Ser1505=
NM_001354905.1:c.4413T>C	NP_001341834.1:p.Ser1471=
NM_001354905.2:c.4413T>C	NP_001341834.1:p.Ser1471=
NM_001354906.1:c.4044T>C	NP_001341835.1:p.Ser1348=
NM_001354906.2:c.4044T>C	NP_001341835.1:p.Ser1348=
ENST00000257430.8:c.4893T>C	ENSP00000257430.4:p.Ser1631=
ENST00000504915.3:c.4947T>C	ENSP00000473355.2:p.Ser1649=
ENST00000505350.2:c.*4899T>C	ENSP00000481752.1:n.*4899T>C
ENST00000507379.6:c.4839T>C	ENSP00000423224.2:p.Ser1613=
ENST00000508376.6:c.4893T>C	ENSP00000427089.2:p.Ser1631=
ENST00000508624.5:c.*4215T>C	ENSP00000424265.1:n.*4215T>C
ENST00000509732.6:c.4893T>C	ENSP00000426541.2:p.Ser1631=
ENST00000512211.7:c.4893T>C	ENSP00000423828.3:p.Ser1631=
ENST00000520401.1:c.230+11515T>C