Canonical Allele Identifier: CA16038561

Gene: APC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843529T>A , CM000667.2:g.112843529T>A	GRCh38
NC_000005.9:g.112179226T>A , CM000667.1:g.112179226T>A	GRCh37
NC_000005.8:g.112207125T>A	NCBI36
NG_008481.4:g.156009T>A , LRG_130:g.156009T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7989T>A	ENSP00000473355.2:p.Tyr2663Ter
ENST00000505350.2:c.*7941T>A	ENSP00000481752.1:n.*7941T>A
ENST00000507379.6:c.7881T>A	ENSP00000423224.2:p.Tyr2627Ter
ENST00000509732.6:c.7935T>A	ENSP00000426541.2:p.Tyr2645Ter
ENST00000512211.7:c.7935T>A	ENSP00000423828.3:p.Tyr2645Ter
ENST00000257430.9:c.7935T>A MANE Select	ENSP00000257430.4:p.Tyr2645Ter
ENST00000257430.8:c.7935T>A	ENSP00000257430.4:p.Tyr2645Ter
ENST00000508376.6:c.7935T>A	ENSP00000427089.2:p.Tyr2645Ter
ENST00000520401.1:c.231-13120T>A
NM_000038.5:c.7935T>A	NP_000029.2:p.Tyr2645Ter
NM_001127510.2:c.7935T>A	NP_001120982.1:p.Tyr2645Ter
NM_001127511.2:c.7881T>A	NP_001120983.2:p.Tyr2627Ter
NM_001354895.1:c.7935T>A	NP_001341824.1:p.Tyr2645Ter
NM_001354896.1:c.7989T>A	NP_001341825.1:p.Tyr2663Ter
NM_001354897.1:c.7965T>A	NP_001341826.1:p.Tyr2655Ter
NM_001354898.1:c.7860T>A	NP_001341827.1:p.Tyr2620Ter
NM_001354899.1:c.7851T>A	NP_001341828.1:p.Tyr2617Ter
NM_001354900.1:c.7812T>A	NP_001341829.1:p.Tyr2604Ter
NM_001354901.1:c.7758T>A	NP_001341830.1:p.Tyr2586Ter
NM_001354902.1:c.7662T>A	NP_001341831.1:p.Tyr2554Ter
NM_001354903.1:c.7632T>A	NP_001341832.1:p.Tyr2544Ter
NM_001354904.1:c.7557T>A	NP_001341833.1:p.Tyr2519Ter
NM_001354905.1:c.7455T>A	NP_001341834.1:p.Tyr2485Ter
NM_001354906.1:c.7086T>A	NP_001341835.1:p.Tyr2362Ter
NM_000038.6:c.7935T>A MANE Select	NP_000029.2:p.Tyr2645Ter
NM_001127510.3:c.7935T>A	NP_001120982.1:p.Tyr2645Ter
NM_001127511.3:c.7881T>A	NP_001120983.2:p.Tyr2627Ter
NM_001354895.2:c.7935T>A	NP_001341824.1:p.Tyr2645Ter
NM_001354896.2:c.7989T>A	NP_001341825.1:p.Tyr2663Ter
NM_001354897.2:c.7965T>A	NP_001341826.1:p.Tyr2655Ter
NM_001354898.2:c.7860T>A	NP_001341827.1:p.Tyr2620Ter
NM_001354899.2:c.7851T>A	NP_001341828.1:p.Tyr2617Ter
NM_001354900.2:c.7812T>A	NP_001341829.1:p.Tyr2604Ter
NM_001354901.2:c.7758T>A	NP_001341830.1:p.Tyr2586Ter
NM_001354902.2:c.7662T>A	NP_001341831.1:p.Tyr2554Ter
NM_001354903.2:c.7632T>A	NP_001341832.1:p.Tyr2544Ter
NM_001354904.2:c.7557T>A	NP_001341833.1:p.Tyr2519Ter
NM_001354905.2:c.7455T>A	NP_001341834.1:p.Tyr2485Ter
NM_001354906.2:c.7086T>A	NP_001341835.1:p.Tyr2362Ter