Canonical Allele Identifier: CA6835180

Gene: ANAPC5

Linked Data

• dbSNP Id: rs763816672
• ExAC: 12:121756249 C / CCTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT
• MyVariant Identifiers: chr12:g.121756249_121756250insCTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT (hg19) ; chr12:g.121318446_121318447insCTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318446_121318447insCTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT , CM000674.2:g.121318446_121318447insCTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT	GRCh38
NC_000012.11:g.121756249_121756250insCTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT , CM000674.1:g.121756249_121756250insCTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT	GRCh37
NC_000012.10:g.120240632_120240633insCTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1746-23_1746-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG MANE Select	ENSP00000261819.3:n.1746-23_1746-22insATATTCCCTAGTACCTTATAGGC...
ENST00000261819.7:c.1746-23_1746-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	ENSP00000261819.3:n.1746-23_1746-22insATATTCCCTAGTACCTTATAGGC...
ENST00000441917.6:c.1410-23_1410-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	ENSP00000415061.2:n.1410-23_1410-22insATATTCCCTAGTACCTTATAGGC...
ENST00000534976.5:n.2455_2456insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG
ENST00000535482.1:c.744-23_744-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	ENSP00000438754.1:n.744-23_744-22insATATTCCCTAGTACCTTATAGGCCC...
ENST00000535641.5:n.1957-23_1957-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG
ENST00000539079.5:c.1090-43_1090-42insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG
ENST00000541887.5:c.1707-23_1707-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	ENSP00000439875.1:n.1707-23_1707-22insATATTCCCTAGTACCTTATAGGC...
ENST00000544314.5:n.864-23_864-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG
ENST00000545218.5:n.988+54_988+55insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG
NM_001137559.1:c.1410-23_1410-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	NP_001131031.1:n.1410-23_1410-22insATATTCCCTAGTACCTTATAGGCCCT...
NM_016237.4:c.1746-23_1746-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	NP_057321.2:n.1746-23_1746-22insATATTCCCTAGTACCTTATAGGCCCTACA...
XM_005253900.2:c.1707-23_1707-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	XP_005253957.1:n.1707-23_1707-22insATATTCCCTAGTACCTTATAGGCCCT...
XM_006719449.1:c.552-23_552-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	XP_006719512.1:n.552-23_552-22insATATTCCCTAGTACCTTATAGGCCCTAC...
NM_001330489.1:c.1707-23_1707-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	NP_001317418.1:n.1707-23_1707-22insATATTCCCTAGTACCTTATAGGCCCT...
XM_017019423.2:c.552-23_552-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	XP_016874912.1:n.552-23_552-22insATATTCCCTAGTACCTTATAGGCCCTAC...
XM_017019424.2:c.552-23_552-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	XP_016874913.1:n.552-23_552-22insATATTCCCTAGTACCTTATAGGCCCTAC...
NM_016237.5:c.1746-23_1746-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG MANE Select	NP_057321.2:n.1746-23_1746-22insATATTCCCTAGTACCTTATAGGCCCTACA...
NM_001330489.2:c.1707-23_1707-22insATATTCCCTAGTACCTTATAGGCCCTACACATAGAAG	NP_001317418.1:n.1707-23_1707-22insATATTCCCTAGTACCTTATAGGCCCT...