Canonical Allele Identifier: CA386959715

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756138T>G (hg19) ; chr12:g.121318335T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318335T>G , CM000674.2:g.121318335T>G	GRCh38
NC_000012.11:g.121756138T>G , CM000674.1:g.121756138T>G	GRCh37
NC_000012.10:g.120240521T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1835A>C MANE Select	ENSP00000261819.3:p.Lys612Thr
ENST00000261819.7:c.1835A>C	ENSP00000261819.3:p.Lys612Thr
ENST00000441917.6:c.1499A>C	ENSP00000415061.2:p.Lys500Thr
ENST00000534976.5:n.2567A>C
ENST00000535482.1:c.833A>C	ENSP00000438754.1:p.Lys278Thr
ENST00000535641.5:n.2046A>C
ENST00000539079.5:c.1159A>C
ENST00000541887.5:c.1796A>C	ENSP00000439875.1:p.Lys599Thr
ENST00000544314.5:n.953A>C
ENST00000545218.5:n.1005A>C
NM_001137559.1:c.1499A>C	NP_001131031.1:p.Lys500Thr
NM_016237.4:c.1835A>C	NP_057321.2:p.Lys612Thr
XM_005253900.2:c.1796A>C	XP_005253957.1:p.Lys599Thr
XM_006719449.1:c.641A>C	XP_006719512.1:p.Lys214Thr
NM_001330489.1:c.1796A>C	NP_001317418.1:p.Lys599Thr
XM_017019423.2:c.641A>C	XP_016874912.1:p.Lys214Thr
XM_017019424.2:c.641A>C	XP_016874913.1:p.Lys214Thr
NM_016237.5:c.1835A>C MANE Select	NP_057321.2:p.Lys612Thr
NM_001330489.2:c.1796A>C	NP_001317418.1:p.Lys599Thr