Canonical Allele Identifier: CA16028657

Gene: APC

Linked Data

• dbSNP Id: rs753209586
• MyVariant Identifiers: chr5:g.112174632G>C (hg19) ; chr5:g.112838935G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838935G>C , CM000667.2:g.112838935G>C	GRCh38
NC_000005.9:g.112174632G>C , CM000667.1:g.112174632G>C	GRCh37
NC_000005.8:g.112202531G>C	NCBI36
NG_008481.4:g.151415G>C , LRG_130:g.151415G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3006G>C	ENSP00000484935.2:n.3006G>C
ENST00000504915.3:c.3395G>C	ENSP00000473355.2:p.Arg1132Pro
ENST00000505350.2:c.*3347G>C	ENSP00000481752.1:n.*3347G>C
ENST00000507379.6:c.3287G>C	ENSP00000423224.2:p.Arg1096Pro
ENST00000509732.6:c.3341G>C	ENSP00000426541.2:p.Arg1114Pro
ENST00000512211.7:c.3341G>C	ENSP00000423828.3:p.Arg1114Pro
ENST00000257430.9:c.3341G>C MANE Select	ENSP00000257430.4:p.Arg1114Pro
ENST00000257430.8:c.3341G>C	ENSP00000257430.4:p.Arg1114Pro
ENST00000502371.2:c.1694G>C
ENST00000507379.5:c.3287G>C	ENSP00000423224.1:p.Arg1096Pro
ENST00000508376.6:c.3341G>C	ENSP00000427089.2:p.Arg1114Pro
ENST00000508624.5:c.*2663G>C	ENSP00000424265.1:n.*2663G>C
ENST00000512211.6:c.3341G>C	ENSP00000423828.2:p.Arg1114Pro
ENST00000520401.1:c.230+9963G>C
NM_000038.5:c.3341G>C	NP_000029.2:p.Arg1114Pro
NM_001127510.2:c.3341G>C	NP_001120982.1:p.Arg1114Pro
NM_001127511.2:c.3287G>C	NP_001120983.2:p.Arg1096Pro
NM_001354895.1:c.3341G>C	NP_001341824.1:p.Arg1114Pro
NM_001354896.1:c.3395G>C	NP_001341825.1:p.Arg1132Pro
NM_001354897.1:c.3371G>C	NP_001341826.1:p.Arg1124Pro
NM_001354898.1:c.3266G>C	NP_001341827.1:p.Arg1089Pro
NM_001354899.1:c.3257G>C	NP_001341828.1:p.Arg1086Pro
NM_001354900.1:c.3218G>C	NP_001341829.1:p.Arg1073Pro
NM_001354901.1:c.3164G>C	NP_001341830.1:p.Arg1055Pro
NM_001354902.1:c.3068G>C	NP_001341831.1:p.Arg1023Pro
NM_001354903.1:c.3038G>C	NP_001341832.1:p.Arg1013Pro
NM_001354904.1:c.2963G>C	NP_001341833.1:p.Arg988Pro
NM_001354905.1:c.2861G>C	NP_001341834.1:p.Arg954Pro
NM_001354906.1:c.2492G>C	NP_001341835.1:p.Arg831Pro
NM_000038.6:c.3341G>C MANE Select	NP_000029.2:p.Arg1114Pro
NM_001127510.3:c.3341G>C	NP_001120982.1:p.Arg1114Pro
NM_001127511.3:c.3287G>C	NP_001120983.2:p.Arg1096Pro
NM_001354895.2:c.3341G>C	NP_001341824.1:p.Arg1114Pro
NM_001354896.2:c.3395G>C	NP_001341825.1:p.Arg1132Pro
NM_001354897.2:c.3371G>C	NP_001341826.1:p.Arg1124Pro
NM_001354898.2:c.3266G>C	NP_001341827.1:p.Arg1089Pro
NM_001354899.2:c.3257G>C	NP_001341828.1:p.Arg1086Pro
NM_001354900.2:c.3218G>C	NP_001341829.1:p.Arg1073Pro
NM_001354901.2:c.3164G>C	NP_001341830.1:p.Arg1055Pro
NM_001354902.2:c.3068G>C	NP_001341831.1:p.Arg1023Pro
NM_001354903.2:c.3038G>C	NP_001341832.1:p.Arg1013Pro
NM_001354904.2:c.2963G>C	NP_001341833.1:p.Arg988Pro
NM_001354905.2:c.2861G>C	NP_001341834.1:p.Arg954Pro
NM_001354906.2:c.2492G>C	NP_001341835.1:p.Arg831Pro