Canonical Allele Identifier: CA171668

Gene: CENPJ

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24906805C>T , CM000675.2:g.24906805C>T	GRCh38
NC_000013.10:g.25480943C>T , CM000675.1:g.25480943C>T	GRCh37
NC_000013.9:g.24378943C>T	NCBI36
NG_009165.2:g.21143G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018451.5:c.1233G>A MANE Select	NP_060921.3:p.Pro411=
ENST00000381884.9:c.1233G>A MANE Select	ENSP00000371308.4:p.Pro411=
NM_018451.4:c.1233G>A	NP_060921.3:p.Pro411=
NR_047594.1:n.1428G>A
NR_047594.2:n.1400G>A
NR_047595.1:n.1428G>A
NR_047595.2:n.1400G>A
ENST00000381884.8:c.1233G>A	ENSP00000371308.4:p.Pro411=
ENST00000545981.5:c.1233G>A	ENSP00000441090.2:p.Pro411=
ENST00000545981.6:c.1233G>A	ENSP00000441090.2:p.Pro411=
ENST00000616936.4:c.1233G>A	ENSP00000477511.1:p.Pro411=
XM_011535149.1:c.1233G>A	XP_011533451.1:p.Pro411=
XM_011535149.2:c.1233G>A	XP_011533451.1:p.Pro411=
XM_011535150.1:c.1233G>A	XP_011533452.1:p.Pro411=
XM_011535150.2:c.1233G>A	XP_011533452.1:p.Pro411=
XM_011535151.1:c.1233G>A	XP_011533453.1:p.Pro411=
XM_017020673.1:c.1233G>A	XP_016876162.1:p.Pro411=
XR_941627.1:n.1428G>A
XR_941628.1:n.1428G>A