Canonical Allele Identifier: CA16027985

Gene: APC

Linked Data

• dbSNP Id: rs1554084654
• MyVariant Identifiers: chr5:g.112174331A>T (hg19) ; chr5:g.112838634A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838634A>T , CM000667.2:g.112838634A>T	GRCh38
NC_000005.9:g.112174331A>T , CM000667.1:g.112174331A>T	GRCh37
NC_000005.8:g.112202230A>T	NCBI36
NG_008481.4:g.151114A>T , LRG_130:g.151114A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2705A>T	ENSP00000484935.2:n.2705A>T
ENST00000504915.3:c.3094A>T	ENSP00000473355.2:p.Met1032Leu
ENST00000505350.2:c.*3046A>T	ENSP00000481752.1:n.*3046A>T
ENST00000507379.6:c.2986A>T	ENSP00000423224.2:p.Met996Leu
ENST00000509732.6:c.3040A>T	ENSP00000426541.2:p.Met1014Leu
ENST00000512211.7:c.3040A>T	ENSP00000423828.3:p.Met1014Leu
ENST00000257430.9:c.3040A>T MANE Select	ENSP00000257430.4:p.Met1014Leu
ENST00000257430.8:c.3040A>T	ENSP00000257430.4:p.Met1014Leu
ENST00000502371.2:c.1393A>T
ENST00000507379.5:c.2986A>T	ENSP00000423224.1:p.Met996Leu
ENST00000508376.6:c.3040A>T	ENSP00000427089.2:p.Met1014Leu
ENST00000508624.5:c.*2362A>T	ENSP00000424265.1:n.*2362A>T
ENST00000512211.6:c.3040A>T	ENSP00000423828.2:p.Met1014Leu
ENST00000520401.1:c.230+9662A>T
NM_000038.5:c.3040A>T	NP_000029.2:p.Met1014Leu
NM_001127510.2:c.3040A>T	NP_001120982.1:p.Met1014Leu
NM_001127511.2:c.2986A>T	NP_001120983.2:p.Met996Leu
NM_001354895.1:c.3040A>T	NP_001341824.1:p.Met1014Leu
NM_001354896.1:c.3094A>T	NP_001341825.1:p.Met1032Leu
NM_001354897.1:c.3070A>T	NP_001341826.1:p.Met1024Leu
NM_001354898.1:c.2965A>T	NP_001341827.1:p.Met989Leu
NM_001354899.1:c.2956A>T	NP_001341828.1:p.Met986Leu
NM_001354900.1:c.2917A>T	NP_001341829.1:p.Met973Leu
NM_001354901.1:c.2863A>T	NP_001341830.1:p.Met955Leu
NM_001354902.1:c.2767A>T	NP_001341831.1:p.Met923Leu
NM_001354903.1:c.2737A>T	NP_001341832.1:p.Met913Leu
NM_001354904.1:c.2662A>T	NP_001341833.1:p.Met888Leu
NM_001354905.1:c.2560A>T	NP_001341834.1:p.Met854Leu
NM_001354906.1:c.2191A>T	NP_001341835.1:p.Met731Leu
NM_000038.6:c.3040A>T MANE Select	NP_000029.2:p.Met1014Leu
NM_001127510.3:c.3040A>T	NP_001120982.1:p.Met1014Leu
NM_001127511.3:c.2986A>T	NP_001120983.2:p.Met996Leu
NM_001354895.2:c.3040A>T	NP_001341824.1:p.Met1014Leu
NM_001354896.2:c.3094A>T	NP_001341825.1:p.Met1032Leu
NM_001354897.2:c.3070A>T	NP_001341826.1:p.Met1024Leu
NM_001354898.2:c.2965A>T	NP_001341827.1:p.Met989Leu
NM_001354899.2:c.2956A>T	NP_001341828.1:p.Met986Leu
NM_001354900.2:c.2917A>T	NP_001341829.1:p.Met973Leu
NM_001354901.2:c.2863A>T	NP_001341830.1:p.Met955Leu
NM_001354902.2:c.2767A>T	NP_001341831.1:p.Met923Leu
NM_001354903.2:c.2737A>T	NP_001341832.1:p.Met913Leu
NM_001354904.2:c.2662A>T	NP_001341833.1:p.Met888Leu
NM_001354905.2:c.2560A>T	NP_001341834.1:p.Met854Leu
NM_001354906.2:c.2191A>T	NP_001341835.1:p.Met731Leu