Canonical Allele Identifier: CA482430264

Gene: ANAPC5

Linked Data

• gnomAD v4: 12-121318315-A-G
• MyVariant Identifiers: chr12:g.121756118A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318315A>G , CM000674.2:g.121318315A>G	GRCh38
NC_000012.11:g.121756118A>G , CM000674.1:g.121756118A>G	GRCh37
NC_000012.10:g.120240501A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1855T>C MANE Select	ENSP00000261819.3:p.Leu619=
ENST00000261819.7:c.1855T>C	ENSP00000261819.3:p.Leu619=
ENST00000441917.6:c.1519T>C	ENSP00000415061.2:p.Leu507=
ENST00000534976.5:n.2587T>C
ENST00000535482.1:c.853T>C	ENSP00000438754.1:p.Leu285=
ENST00000535641.5:n.2066T>C
ENST00000539079.5:c.1179T>C
ENST00000541887.5:c.1816T>C	ENSP00000439875.1:p.Leu606=
ENST00000544314.5:n.973T>C
ENST00000545218.5:n.1025T>C
NM_001137559.1:c.1519T>C	NP_001131031.1:p.Leu507=
NM_016237.4:c.1855T>C	NP_057321.2:p.Leu619=
XM_005253900.2:c.1816T>C	XP_005253957.1:p.Leu606=
XM_006719449.1:c.661T>C	XP_006719512.1:p.Leu221=
NM_001330489.1:c.1816T>C	NP_001317418.1:p.Leu606=
XM_017019423.2:c.661T>C	XP_016874912.1:p.Leu221=
XM_017019424.2:c.661T>C	XP_016874913.1:p.Leu221=
NM_016237.5:c.1855T>C MANE Select	NP_057321.2:p.Leu619=
NM_001330489.2:c.1816T>C	NP_001317418.1:p.Leu606=