Canonical Allele Identifier: CA387585186

Gene: CENPJ

Linked Data

• dbSNP Id: rs1954515647
• MyVariant Identifiers: chr13:g.25479814G>T (hg19) ; chr13:g.24905676G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24905676G>T , CM000675.2:g.24905676G>T	GRCh38
NC_000013.10:g.25479814G>T , CM000675.1:g.25479814G>T	GRCh37
NC_000013.9:g.24377814G>T	NCBI36
NG_009165.2:g.22272C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.2362C>A MANE Select	ENSP00000371308.4:p.Leu788Met
ENST00000545981.6:c.2362C>A	ENSP00000441090.2:p.Leu788Met
ENST00000381884.8:c.2362C>A	ENSP00000371308.4:p.Leu788Met
ENST00000545981.5:c.2362C>A	ENSP00000441090.2:p.Leu788Met
ENST00000616936.4:c.2362C>A	ENSP00000477511.1:p.Leu788Met
NM_018451.4:c.2362C>A	NP_060921.3:p.Leu788Met
NR_047594.1:n.2557C>A
NR_047595.1:n.2557C>A
XM_011535149.1:c.2362C>A	XP_011533451.1:p.Leu788Met
XM_011535150.1:c.2362C>A	XP_011533452.1:p.Leu788Met
XM_011535151.1:c.2362C>A	XP_011533453.1:p.Leu788Met
XR_941627.1:n.2557C>A
XR_941628.1:n.2557C>A
XM_011535149.2:c.2362C>A	XP_011533451.1:p.Leu788Met
XM_011535150.2:c.2362C>A	XP_011533452.1:p.Leu788Met
XM_017020673.1:c.2362C>A	XP_016876162.1:p.Leu788Met
NM_018451.5:c.2362C>A MANE Select	NP_060921.3:p.Leu788Met
NR_047594.2:n.2529C>A
NR_047595.2:n.2529C>A