Canonical Allele Identifier: CA2622386685

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883259-C-CCGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883260_24883263dup , CM000675.2:g.24883260_24883263dup	GRCh38
NC_000013.10:g.25457398_25457401dup , CM000675.1:g.25457398_25457401dup	GRCh37
NC_000013.9:g.24355398_24355401dup	NCBI36
NG_009165.2:g.44685_44688dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3931_3934dup (CENPJ) MANE Select	ENSP00000371308.4:p.Gly1312GlufsTer16
ENST00000545981.6:c.*671_*674dup (CENPJ)	ENSP00000441090.2:n.*671_*674dup
ENST00000381884.8:c.3931_3934dup (CENPJ)	ENSP00000371308.4:p.Gly1312GlufsTer16
ENST00000545981.5:c.*672_*675dup (CENPJ)	ENSP00000441090.2:n.*672_*675dup
ENST00000616936.4:c.*585_*588dup (CENPJ)	ENSP00000477511.1:n.*585_*588dup
NM_018451.4:c.3931_3934dup (CENPJ)	NP_060921.3:p.Gly1312GlufsTer16
NR_047594.1:n.4243_4246dup (CENPJ)
NR_047595.1:n.4041_4044dup (CENPJ)
XM_011535156.1:c.*10+3965_*10+3968dup (RNF17)	XP_011533458.1:n.*10+3965_*10+3968dup
XM_011535156.2:c.*10+3965_*10+3968dup (RNF17)	XP_011533458.1:n.*10+3965_*10+3968dup
NM_018451.5:c.3931_3934dup (CENPJ) MANE Select	NP_060921.3:p.Gly1312GlufsTer16
NR_047594.2:n.4215_4218dup (CENPJ)
NR_047595.2:n.4013_4016dup (CENPJ)