Canonical Allele Identifier: CA387584949

Gene: CENPJ

Linked Data

• gnomAD v4: 13-24905577-T-A
• MyVariant Identifiers: chr13:g.25479715T>A (hg19) ; chr13:g.24905577T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24905577T>A , CM000675.2:g.24905577T>A	GRCh38
NC_000013.10:g.25479715T>A , CM000675.1:g.25479715T>A	GRCh37
NC_000013.9:g.24377715T>A	NCBI36
NG_009165.2:g.22371A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.2461A>T MANE Select	ENSP00000371308.4:p.Thr821Ser
ENST00000545981.6:c.2461A>T	ENSP00000441090.2:p.Thr821Ser
ENST00000381884.8:c.2461A>T	ENSP00000371308.4:p.Thr821Ser
ENST00000545981.5:c.2461A>T	ENSP00000441090.2:p.Thr821Ser
ENST00000616936.4:c.2461A>T	ENSP00000477511.1:p.Thr821Ser
NM_018451.4:c.2461A>T	NP_060921.3:p.Thr821Ser
NR_047594.1:n.2656A>T
NR_047595.1:n.2656A>T
XM_011535149.1:c.2461A>T	XP_011533451.1:p.Thr821Ser
XM_011535150.1:c.2461A>T	XP_011533452.1:p.Thr821Ser
XM_011535151.1:c.2461A>T	XP_011533453.1:p.Thr821Ser
XR_941627.1:n.2656A>T
XR_941628.1:n.2656A>T
XM_011535149.2:c.2461A>T	XP_011533451.1:p.Thr821Ser
XM_011535150.2:c.2461A>T	XP_011533452.1:p.Thr821Ser
XM_017020673.1:c.2461A>T	XP_016876162.1:p.Thr821Ser
NM_018451.5:c.2461A>T MANE Select	NP_060921.3:p.Thr821Ser
NR_047594.2:n.2628A>T
NR_047595.2:n.2628A>T