Canonical Allele Identifier: CA804629480

Gene: UBE2D2

Linked Data

• dbSNP Id: rs1402096909
• MyVariant Identifiers: chr5:g.138949213_138949216del (hg19) ; chr5:g.139569628_139569631del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139569632_139569635del , CM000667.2:g.139569632_139569635del	GRCh38
NC_000005.9:g.138949217_138949220del , CM000667.1:g.138949217_138949220del	GRCh37
NC_000005.8:g.138929401_138929404del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000698321.1:c.-162+7225_-162+7228del	ENSP00000513666.1:n.-162+7225_-162+7228del
ENST00000398733.8:c.24+7817_24+7820del MANE Select	ENSP00000381717.3:n.24+7817_24+7820del
ENST00000398733.7:c.24+7817_24+7820del	ENSP00000381717.3:n.24+7817_24+7820del
ENST00000398734.8:c.24+7817_24+7820del	ENSP00000381718.4:n.24+7817_24+7820del
ENST00000505007.5:c.-64+7225_-64+7228del	ENSP00000426523.1:n.-64+7225_-64+7228del
ENST00000505548.5:c.-64+7225_-64+7228del	ENSP00000424941.1:n.-64+7225_-64+7228del
ENST00000510470.1:n.92+7817_92+7820del
ENST00000511725.5:c.-63-30740_-63-30737del	ENSP00000429613.1:n.-63-30740_-63-30737del
NM_003339.2:c.24+7817_24+7820del	NP_003330.1:n.24+7817_24+7820del
NM_181838.1:c.-64+7225_-64+7228del	NP_862821.1:n.-64+7225_-64+7228del
XM_017009820.1:c.-96+7001_-96+7004del	XP_016865309.1:n.-96+7001_-96+7004del
NM_003339.3:c.24+7817_24+7820del MANE Select	NP_003330.1:n.24+7817_24+7820del
NM_181838.2:c.-64+7225_-64+7228del	NP_862821.1:n.-64+7225_-64+7228del