Canonical Allele Identifier: CA16025428

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112170783A>T (hg19) ; chr5:g.112835086A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835086A>T , CM000667.2:g.112835086A>T	GRCh38
NC_000005.9:g.112170783A>T , CM000667.1:g.112170783A>T	GRCh37
NC_000005.8:g.112198682A>T	NCBI36
NG_008481.4:g.147566A>T , LRG_130:g.147566A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1544A>T	ENSP00000484935.2:n.1544A>T
ENST00000504915.3:c.1933A>T	ENSP00000473355.2:p.Asn645Tyr
ENST00000505350.2:c.*1885A>T	ENSP00000481752.1:n.*1885A>T
ENST00000507379.6:c.1825A>T	ENSP00000423224.2:p.Asn609Tyr
ENST00000509732.6:c.1879A>T	ENSP00000426541.2:p.Asn627Tyr
ENST00000512211.7:c.1879A>T	ENSP00000423828.3:p.Asn627Tyr
ENST00000257430.9:c.1879A>T MANE Select	ENSP00000257430.4:p.Asn627Tyr
ENST00000257430.8:c.1879A>T	ENSP00000257430.4:p.Asn627Tyr
ENST00000502371.2:c.232A>T
ENST00000504915.2:c.568A>T	ENSP00000473355.1:p.Asn190Tyr
ENST00000507379.5:c.1825A>T	ENSP00000423224.1:p.Asn609Tyr
ENST00000508376.6:c.1879A>T	ENSP00000427089.2:p.Asn627Tyr
ENST00000508624.5:c.*1201A>T	ENSP00000424265.1:n.*1201A>T
ENST00000512211.6:c.1879A>T	ENSP00000423828.2:p.Asn627Tyr
ENST00000520401.1:c.230+6114A>T
NM_000038.5:c.1879A>T	NP_000029.2:p.Asn627Tyr
NM_001127510.2:c.1879A>T	NP_001120982.1:p.Asn627Tyr
NM_001127511.2:c.1825A>T	NP_001120983.2:p.Asn609Tyr
NM_001354895.1:c.1879A>T	NP_001341824.1:p.Asn627Tyr
NM_001354896.1:c.1933A>T	NP_001341825.1:p.Asn645Tyr
NM_001354897.1:c.1909A>T	NP_001341826.1:p.Asn637Tyr
NM_001354898.1:c.1804A>T	NP_001341827.1:p.Asn602Tyr
NM_001354899.1:c.1795A>T	NP_001341828.1:p.Asn599Tyr
NM_001354900.1:c.1756A>T	NP_001341829.1:p.Asn586Tyr
NM_001354901.1:c.1702A>T	NP_001341830.1:p.Asn568Tyr
NM_001354902.1:c.1606A>T	NP_001341831.1:p.Asn536Tyr
NM_001354903.1:c.1576A>T	NP_001341832.1:p.Asn526Tyr
NM_001354904.1:c.1501A>T	NP_001341833.1:p.Asn501Tyr
NM_001354905.1:c.1399A>T	NP_001341834.1:p.Asn467Tyr
NM_001354906.1:c.1030A>T	NP_001341835.1:p.Asn344Tyr
NM_000038.6:c.1879A>T MANE Select	NP_000029.2:p.Asn627Tyr
NM_001127510.3:c.1879A>T	NP_001120982.1:p.Asn627Tyr
NM_001127511.3:c.1825A>T	NP_001120983.2:p.Asn609Tyr
NM_001354895.2:c.1879A>T	NP_001341824.1:p.Asn627Tyr
NM_001354896.2:c.1933A>T	NP_001341825.1:p.Asn645Tyr
NM_001354897.2:c.1909A>T	NP_001341826.1:p.Asn637Tyr
NM_001354898.2:c.1804A>T	NP_001341827.1:p.Asn602Tyr
NM_001354899.2:c.1795A>T	NP_001341828.1:p.Asn599Tyr
NM_001354900.2:c.1756A>T	NP_001341829.1:p.Asn586Tyr
NM_001354901.2:c.1702A>T	NP_001341830.1:p.Asn568Tyr
NM_001354902.2:c.1606A>T	NP_001341831.1:p.Asn536Tyr
NM_001354903.2:c.1576A>T	NP_001341832.1:p.Asn526Tyr
NM_001354904.2:c.1501A>T	NP_001341833.1:p.Asn501Tyr
NM_001354905.2:c.1399A>T	NP_001341834.1:p.Asn467Tyr
NM_001354906.2:c.1030A>T	NP_001341835.1:p.Asn344Tyr