Canonical Allele Identifier: CA16028676

Gene: APC

Linked Data

• dbSNP Id: rs140493115
• MyVariant Identifiers: chr5:g.112174643A>T (hg19) ; chr5:g.112838946A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838946A>T , CM000667.2:g.112838946A>T	GRCh38
NC_000005.9:g.112174643A>T , CM000667.1:g.112174643A>T	GRCh37
NC_000005.8:g.112202542A>T	NCBI36
NG_008481.4:g.151426A>T , LRG_130:g.151426A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3017A>T	ENSP00000484935.2:n.3017A>T
ENST00000504915.3:c.3406A>T	ENSP00000473355.2:p.Asn1136Tyr
ENST00000505350.2:c.*3358A>T	ENSP00000481752.1:n.*3358A>T
ENST00000507379.6:c.3298A>T	ENSP00000423224.2:p.Asn1100Tyr
ENST00000509732.6:c.3352A>T	ENSP00000426541.2:p.Asn1118Tyr
ENST00000512211.7:c.3352A>T	ENSP00000423828.3:p.Asn1118Tyr
ENST00000257430.9:c.3352A>T MANE Select	ENSP00000257430.4:p.Asn1118Tyr
ENST00000257430.8:c.3352A>T	ENSP00000257430.4:p.Asn1118Tyr
ENST00000502371.2:c.1705A>T
ENST00000507379.5:c.3298A>T	ENSP00000423224.1:p.Asn1100Tyr
ENST00000508376.6:c.3352A>T	ENSP00000427089.2:p.Asn1118Tyr
ENST00000508624.5:c.*2674A>T	ENSP00000424265.1:n.*2674A>T
ENST00000512211.6:c.3352A>T	ENSP00000423828.2:p.Asn1118Tyr
ENST00000520401.1:c.230+9974A>T
NM_000038.5:c.3352A>T	NP_000029.2:p.Asn1118Tyr
NM_001127510.2:c.3352A>T	NP_001120982.1:p.Asn1118Tyr
NM_001127511.2:c.3298A>T	NP_001120983.2:p.Asn1100Tyr
NM_001354895.1:c.3352A>T	NP_001341824.1:p.Asn1118Tyr
NM_001354896.1:c.3406A>T	NP_001341825.1:p.Asn1136Tyr
NM_001354897.1:c.3382A>T	NP_001341826.1:p.Asn1128Tyr
NM_001354898.1:c.3277A>T	NP_001341827.1:p.Asn1093Tyr
NM_001354899.1:c.3268A>T	NP_001341828.1:p.Asn1090Tyr
NM_001354900.1:c.3229A>T	NP_001341829.1:p.Asn1077Tyr
NM_001354901.1:c.3175A>T	NP_001341830.1:p.Asn1059Tyr
NM_001354902.1:c.3079A>T	NP_001341831.1:p.Asn1027Tyr
NM_001354903.1:c.3049A>T	NP_001341832.1:p.Asn1017Tyr
NM_001354904.1:c.2974A>T	NP_001341833.1:p.Asn992Tyr
NM_001354905.1:c.2872A>T	NP_001341834.1:p.Asn958Tyr
NM_001354906.1:c.2503A>T	NP_001341835.1:p.Asn835Tyr
NM_000038.6:c.3352A>T MANE Select	NP_000029.2:p.Asn1118Tyr
NM_001127510.3:c.3352A>T	NP_001120982.1:p.Asn1118Tyr
NM_001127511.3:c.3298A>T	NP_001120983.2:p.Asn1100Tyr
NM_001354895.2:c.3352A>T	NP_001341824.1:p.Asn1118Tyr
NM_001354896.2:c.3406A>T	NP_001341825.1:p.Asn1136Tyr
NM_001354897.2:c.3382A>T	NP_001341826.1:p.Asn1128Tyr
NM_001354898.2:c.3277A>T	NP_001341827.1:p.Asn1093Tyr
NM_001354899.2:c.3268A>T	NP_001341828.1:p.Asn1090Tyr
NM_001354900.2:c.3229A>T	NP_001341829.1:p.Asn1077Tyr
NM_001354901.2:c.3175A>T	NP_001341830.1:p.Asn1059Tyr
NM_001354902.2:c.3079A>T	NP_001341831.1:p.Asn1027Tyr
NM_001354903.2:c.3049A>T	NP_001341832.1:p.Asn1017Tyr
NM_001354904.2:c.2974A>T	NP_001341833.1:p.Asn992Tyr
NM_001354905.2:c.2872A>T	NP_001341834.1:p.Asn958Tyr
NM_001354906.2:c.2503A>T	NP_001341835.1:p.Asn835Tyr