Canonical Allele Identifier: CA16028064

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174365T>C (hg19) ; chr5:g.112838668T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838668T>C , CM000667.2:g.112838668T>C	GRCh38
NC_000005.9:g.112174365T>C , CM000667.1:g.112174365T>C	GRCh37
NC_000005.8:g.112202264T>C	NCBI36
NG_008481.4:g.151148T>C , LRG_130:g.151148T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2739T>C	ENSP00000484935.2:n.2739T>C
ENST00000504915.3:c.3128T>C	ENSP00000473355.2:p.Ile1043Thr
ENST00000505350.2:c.*3080T>C	ENSP00000481752.1:n.*3080T>C
ENST00000507379.6:c.3020T>C	ENSP00000423224.2:p.Ile1007Thr
ENST00000509732.6:c.3074T>C	ENSP00000426541.2:p.Ile1025Thr
ENST00000512211.7:c.3074T>C	ENSP00000423828.3:p.Ile1025Thr
ENST00000257430.9:c.3074T>C MANE Select	ENSP00000257430.4:p.Ile1025Thr
ENST00000257430.8:c.3074T>C	ENSP00000257430.4:p.Ile1025Thr
ENST00000502371.2:c.1427T>C
ENST00000507379.5:c.3020T>C	ENSP00000423224.1:p.Ile1007Thr
ENST00000508376.6:c.3074T>C	ENSP00000427089.2:p.Ile1025Thr
ENST00000508624.5:c.*2396T>C	ENSP00000424265.1:n.*2396T>C
ENST00000512211.6:c.3074T>C	ENSP00000423828.2:p.Ile1025Thr
ENST00000520401.1:c.230+9696T>C
NM_000038.5:c.3074T>C	NP_000029.2:p.Ile1025Thr
NM_001127510.2:c.3074T>C	NP_001120982.1:p.Ile1025Thr
NM_001127511.2:c.3020T>C	NP_001120983.2:p.Ile1007Thr
NM_001354895.1:c.3074T>C	NP_001341824.1:p.Ile1025Thr
NM_001354896.1:c.3128T>C	NP_001341825.1:p.Ile1043Thr
NM_001354897.1:c.3104T>C	NP_001341826.1:p.Ile1035Thr
NM_001354898.1:c.2999T>C	NP_001341827.1:p.Ile1000Thr
NM_001354899.1:c.2990T>C	NP_001341828.1:p.Ile997Thr
NM_001354900.1:c.2951T>C	NP_001341829.1:p.Ile984Thr
NM_001354901.1:c.2897T>C	NP_001341830.1:p.Ile966Thr
NM_001354902.1:c.2801T>C	NP_001341831.1:p.Ile934Thr
NM_001354903.1:c.2771T>C	NP_001341832.1:p.Ile924Thr
NM_001354904.1:c.2696T>C	NP_001341833.1:p.Ile899Thr
NM_001354905.1:c.2594T>C	NP_001341834.1:p.Ile865Thr
NM_001354906.1:c.2225T>C	NP_001341835.1:p.Ile742Thr
NM_000038.6:c.3074T>C MANE Select	NP_000029.2:p.Ile1025Thr
NM_001127510.3:c.3074T>C	NP_001120982.1:p.Ile1025Thr
NM_001127511.3:c.3020T>C	NP_001120983.2:p.Ile1007Thr
NM_001354895.2:c.3074T>C	NP_001341824.1:p.Ile1025Thr
NM_001354896.2:c.3128T>C	NP_001341825.1:p.Ile1043Thr
NM_001354897.2:c.3104T>C	NP_001341826.1:p.Ile1035Thr
NM_001354898.2:c.2999T>C	NP_001341827.1:p.Ile1000Thr
NM_001354899.2:c.2990T>C	NP_001341828.1:p.Ile997Thr
NM_001354900.2:c.2951T>C	NP_001341829.1:p.Ile984Thr
NM_001354901.2:c.2897T>C	NP_001341830.1:p.Ile966Thr
NM_001354902.2:c.2801T>C	NP_001341831.1:p.Ile934Thr
NM_001354903.2:c.2771T>C	NP_001341832.1:p.Ile924Thr
NM_001354904.2:c.2696T>C	NP_001341833.1:p.Ile899Thr
NM_001354905.2:c.2594T>C	NP_001341834.1:p.Ile865Thr
NM_001354906.2:c.2225T>C	NP_001341835.1:p.Ile742Thr