Canonical Allele Identifier: CA696759616

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1408554943
• gnomAD v3: 13-24883110-C-T
• gnomAD v4: 13-24883110-C-T
• MyVariant Identifiers: chr13:g.25457248C>T (hg19) ; chr13:g.24883110C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883110C>T , CM000675.2:g.24883110C>T	GRCh38
NC_000013.10:g.25457248C>T , CM000675.1:g.25457248C>T	GRCh37
NC_000013.9:g.24355248C>T	NCBI36
NG_009165.2:g.44838G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*67G>A (CENPJ) MANE Select	ENSP00000371308.4:n.*67G>A
ENST00000381884.8:c.*67G>A (CENPJ)	ENSP00000371308.4:n.*67G>A
ENST00000616936.4:c.*738G>A (CENPJ)	ENSP00000477511.1:n.*738G>A
NM_018451.4:c.*67G>A (CENPJ)	NP_060921.3:n.*67G>A
NR_047594.1:n.4396G>A (CENPJ)
NR_047595.1:n.4194G>A (CENPJ)
XM_011535156.1:c.*10+3815C>T (RNF17)	XP_011533458.1:n.*10+3815C>T
XM_011535156.2:c.*10+3815C>T (RNF17)	XP_011533458.1:n.*10+3815C>T
NM_018451.5:c.*67G>A (CENPJ) MANE Select	NP_060921.3:n.*67G>A
NR_047594.2:n.4368G>A (CENPJ)
NR_047595.2:n.4166G>A (CENPJ)