Canonical Allele Identifier: CA2594415383

Gene: RNF39

Linked Data

• gnomAD v3: 6-30072961-TTTCAGAC-T
• gnomAD v4: 6-30072961-TTTCAGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30072965_30072971del , CM000668.2:g.30072965_30072971del	GRCh38
NC_000006.11:g.30040742_30040748del , CM000668.1:g.30040742_30040748del	GRCh37
NC_000006.10:g.30148721_30148727del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244360.8:c.478+189_478+195del MANE Select	ENSP00000244360.7:n.478+189_478+195del
ENST00000244360.7:c.478+189_478+195del	ENSP00000244360.7:n.478+189_478+195del
ENST00000376751.8:c.478+189_478+195del	ENSP00000365942.4:n.478+189_478+195del
ENST00000244360.6:c.682+189_682+195del	ENSP00000244360.6:n.682+189_682+195del
ENST00000376751.7:c.682+189_682+195del	ENSP00000365942.3:n.682+189_682+195del
NM_025236.3:c.682+189_682+195del	NP_079512.2:n.682+189_682+195del
NM_170769.2:c.682+189_682+195del	NP_739575.2:n.682+189_682+195del
XM_017011325.1:c.223+189_223+195del	XP_016866814.1:n.223+189_223+195del
XM_017011326.1:c.682+189_682+195del	XP_016866815.1:n.682+189_682+195del
NM_025236.4:c.478+189_478+195del MANE Select	NP_079512.3:n.478+189_478+195del
NM_170769.3:c.478+189_478+195del	NP_739575.3:n.478+189_478+195del