Canonical Allele Identifier: CA2622386669

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883145-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883145G>T , CM000675.2:g.24883145G>T	GRCh38
NC_000013.10:g.25457283G>T , CM000675.1:g.25457283G>T	GRCh37
NC_000013.9:g.24355283G>T	NCBI36
NG_009165.2:g.44803C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*32C>A (CENPJ) MANE Select	ENSP00000371308.4:n.*32C>A
ENST00000381884.8:c.*32C>A (CENPJ)	ENSP00000371308.4:n.*32C>A
ENST00000616936.4:c.*703C>A (CENPJ)	ENSP00000477511.1:n.*703C>A
NM_018451.4:c.*32C>A (CENPJ)	NP_060921.3:n.*32C>A
NR_047594.1:n.4361C>A (CENPJ)
NR_047595.1:n.4159C>A (CENPJ)
XM_011535156.1:c.*10+3850G>T (RNF17)	XP_011533458.1:n.*10+3850G>T
XM_011535156.2:c.*10+3850G>T (RNF17)	XP_011533458.1:n.*10+3850G>T
NM_018451.5:c.*32C>A (CENPJ) MANE Select	NP_060921.3:n.*32C>A
NR_047594.2:n.4333C>A (CENPJ)
NR_047595.2:n.4131C>A (CENPJ)