Canonical Allele Identifier: CA387585062

Gene: CENPJ

Linked Data

• gnomAD v4: 13-24905625-T-C
• MyVariant Identifiers: chr13:g.25479763T>C (hg19) ; chr13:g.24905625T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24905625T>C , CM000675.2:g.24905625T>C	GRCh38
NC_000013.10:g.25479763T>C , CM000675.1:g.25479763T>C	GRCh37
NC_000013.9:g.24377763T>C	NCBI36
NG_009165.2:g.22323A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.2413A>G MANE Select	ENSP00000371308.4:p.Asn805Asp
ENST00000545981.6:c.2413A>G	ENSP00000441090.2:p.Asn805Asp
ENST00000381884.8:c.2413A>G	ENSP00000371308.4:p.Asn805Asp
ENST00000545981.5:c.2413A>G	ENSP00000441090.2:p.Asn805Asp
ENST00000616936.4:c.2413A>G	ENSP00000477511.1:p.Asn805Asp
NM_018451.4:c.2413A>G	NP_060921.3:p.Asn805Asp
NR_047594.1:n.2608A>G
NR_047595.1:n.2608A>G
XM_011535149.1:c.2413A>G	XP_011533451.1:p.Asn805Asp
XM_011535150.1:c.2413A>G	XP_011533452.1:p.Asn805Asp
XM_011535151.1:c.2413A>G	XP_011533453.1:p.Asn805Asp
XR_941627.1:n.2608A>G
XR_941628.1:n.2608A>G
XM_011535149.2:c.2413A>G	XP_011533451.1:p.Asn805Asp
XM_011535150.2:c.2413A>G	XP_011533452.1:p.Asn805Asp
XM_017020673.1:c.2413A>G	XP_016876162.1:p.Asn805Asp
NM_018451.5:c.2413A>G MANE Select	NP_060921.3:p.Asn805Asp
NR_047594.2:n.2580A>G
NR_047595.2:n.2580A>G