Canonical Allele Identifier: CA2622386568

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883041-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883041C>T , CM000675.2:g.24883041C>T	GRCh38
NC_000013.10:g.25457179C>T , CM000675.1:g.25457179C>T	GRCh37
NC_000013.9:g.24355179C>T	NCBI36
NG_009165.2:g.44907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*136G>A (CENPJ) MANE Select	ENSP00000371308.4:n.*136G>A
ENST00000381884.8:c.*136G>A (CENPJ)	ENSP00000371308.4:n.*136G>A
ENST00000616936.4:c.*807G>A (CENPJ)	ENSP00000477511.1:n.*807G>A
NM_018451.4:c.*136G>A (CENPJ)	NP_060921.3:n.*136G>A
NR_047594.1:n.4465G>A (CENPJ)
NR_047595.1:n.4263G>A (CENPJ)
XM_011535156.1:c.*10+3746C>T (RNF17)	XP_011533458.1:n.*10+3746C>T
XM_011535156.2:c.*10+3746C>T (RNF17)	XP_011533458.1:n.*10+3746C>T
NM_018451.5:c.*136G>A (CENPJ) MANE Select	NP_060921.3:n.*136G>A
NR_047594.2:n.4437G>A (CENPJ)
NR_047595.2:n.4235G>A (CENPJ)