Canonical Allele Identifier: CA696759398

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1347899574
• gnomAD v3: 13-24882869-T-A
• gnomAD v4: 13-24882869-T-A
• MyVariant Identifiers: chr13:g.25457007T>A (hg19) ; chr13:g.24882869T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882869T>A , CM000675.2:g.24882869T>A	GRCh38
NC_000013.10:g.25457007T>A , CM000675.1:g.25457007T>A	GRCh37
NC_000013.9:g.24355007T>A	NCBI36
NG_009165.2:g.45079A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*308A>T (CENPJ) MANE Select	ENSP00000371308.4:n.*308A>T
ENST00000616936.4:c.*979A>T (CENPJ)	ENSP00000477511.1:n.*979A>T
NM_018451.4:c.*308A>T (CENPJ)	NP_060921.3:n.*308A>T
NR_047594.1:n.4637A>T (CENPJ)
NR_047595.1:n.4435A>T (CENPJ)
XM_011535156.1:c.*10+3574T>A (RNF17)	XP_011533458.1:n.*10+3574T>A
XM_011535156.2:c.*10+3574T>A (RNF17)	XP_011533458.1:n.*10+3574T>A
NM_018451.5:c.*308A>T (CENPJ) MANE Select	NP_060921.3:n.*308A>T
NR_047594.2:n.4609A>T (CENPJ)
NR_047595.2:n.4407A>T (CENPJ)