Canonical Allele Identifier: CA387594602

Gene: CENPJ RNF17

Linked Data

• MyVariant Identifiers: chr13:g.25457395G>T (hg19) ; chr13:g.24883257G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883257G>T , CM000675.2:g.24883257G>T	GRCh38
NC_000013.10:g.25457395G>T , CM000675.1:g.25457395G>T	GRCh37
NC_000013.9:g.24355395G>T	NCBI36
NG_009165.2:g.44691C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3937C>A (CENPJ) MANE Select	ENSP00000371308.4:p.His1313Asn
ENST00000545981.6:c.*677C>A (CENPJ)	ENSP00000441090.2:n.*677C>A
ENST00000381884.8:c.3937C>A (CENPJ)	ENSP00000371308.4:p.His1313Asn
ENST00000545981.5:c.*678C>A (CENPJ)	ENSP00000441090.2:n.*678C>A
ENST00000616936.4:c.*591C>A (CENPJ)	ENSP00000477511.1:n.*591C>A
NM_018451.4:c.3937C>A (CENPJ)	NP_060921.3:p.His1313Asn
NR_047594.1:n.4249C>A (CENPJ)
NR_047595.1:n.4047C>A (CENPJ)
XM_011535156.1:c.*10+3962G>T (RNF17)	XP_011533458.1:n.*10+3962G>T
XM_011535156.2:c.*10+3962G>T (RNF17)	XP_011533458.1:n.*10+3962G>T
NM_018451.5:c.3937C>A (CENPJ) MANE Select	NP_060921.3:p.His1313Asn
NR_047594.2:n.4221C>A (CENPJ)
NR_047595.2:n.4019C>A (CENPJ)