Canonical Allele Identifier: CA16028072

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174368A>T (hg19) ; chr5:g.112838671A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838671A>T , CM000667.2:g.112838671A>T	GRCh38
NC_000005.9:g.112174368A>T , CM000667.1:g.112174368A>T	GRCh37
NC_000005.8:g.112202267A>T	NCBI36
NG_008481.4:g.151151A>T , LRG_130:g.151151A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2742A>T	ENSP00000484935.2:n.2742A>T
ENST00000504915.3:c.3131A>T	ENSP00000473355.2:p.Asn1044Ile
ENST00000505350.2:c.*3083A>T	ENSP00000481752.1:n.*3083A>T
ENST00000507379.6:c.3023A>T	ENSP00000423224.2:p.Asn1008Ile
ENST00000509732.6:c.3077A>T	ENSP00000426541.2:p.Asn1026Ile
ENST00000512211.7:c.3077A>T	ENSP00000423828.3:p.Asn1026Ile
ENST00000257430.9:c.3077A>T MANE Select	ENSP00000257430.4:p.Asn1026Ile
ENST00000257430.8:c.3077A>T	ENSP00000257430.4:p.Asn1026Ile
ENST00000502371.2:c.1430A>T
ENST00000507379.5:c.3023A>T	ENSP00000423224.1:p.Asn1008Ile
ENST00000508376.6:c.3077A>T	ENSP00000427089.2:p.Asn1026Ile
ENST00000508624.5:c.*2399A>T	ENSP00000424265.1:n.*2399A>T
ENST00000512211.6:c.3077A>T	ENSP00000423828.2:p.Asn1026Ile
ENST00000520401.1:c.230+9699A>T
NM_000038.5:c.3077A>T	NP_000029.2:p.Asn1026Ile
NM_001127510.2:c.3077A>T	NP_001120982.1:p.Asn1026Ile
NM_001127511.2:c.3023A>T	NP_001120983.2:p.Asn1008Ile
NM_001354895.1:c.3077A>T	NP_001341824.1:p.Asn1026Ile
NM_001354896.1:c.3131A>T	NP_001341825.1:p.Asn1044Ile
NM_001354897.1:c.3107A>T	NP_001341826.1:p.Asn1036Ile
NM_001354898.1:c.3002A>T	NP_001341827.1:p.Asn1001Ile
NM_001354899.1:c.2993A>T	NP_001341828.1:p.Asn998Ile
NM_001354900.1:c.2954A>T	NP_001341829.1:p.Asn985Ile
NM_001354901.1:c.2900A>T	NP_001341830.1:p.Asn967Ile
NM_001354902.1:c.2804A>T	NP_001341831.1:p.Asn935Ile
NM_001354903.1:c.2774A>T	NP_001341832.1:p.Asn925Ile
NM_001354904.1:c.2699A>T	NP_001341833.1:p.Asn900Ile
NM_001354905.1:c.2597A>T	NP_001341834.1:p.Asn866Ile
NM_001354906.1:c.2228A>T	NP_001341835.1:p.Asn743Ile
NM_000038.6:c.3077A>T MANE Select	NP_000029.2:p.Asn1026Ile
NM_001127510.3:c.3077A>T	NP_001120982.1:p.Asn1026Ile
NM_001127511.3:c.3023A>T	NP_001120983.2:p.Asn1008Ile
NM_001354895.2:c.3077A>T	NP_001341824.1:p.Asn1026Ile
NM_001354896.2:c.3131A>T	NP_001341825.1:p.Asn1044Ile
NM_001354897.2:c.3107A>T	NP_001341826.1:p.Asn1036Ile
NM_001354898.2:c.3002A>T	NP_001341827.1:p.Asn1001Ile
NM_001354899.2:c.2993A>T	NP_001341828.1:p.Asn998Ile
NM_001354900.2:c.2954A>T	NP_001341829.1:p.Asn985Ile
NM_001354901.2:c.2900A>T	NP_001341830.1:p.Asn967Ile
NM_001354902.2:c.2804A>T	NP_001341831.1:p.Asn935Ile
NM_001354903.2:c.2774A>T	NP_001341832.1:p.Asn925Ile
NM_001354904.2:c.2699A>T	NP_001341833.1:p.Asn900Ile
NM_001354905.2:c.2597A>T	NP_001341834.1:p.Asn866Ile
NM_001354906.2:c.2228A>T	NP_001341835.1:p.Asn743Ile