Canonical Allele Identifier: CA2616232433
Gene: CD3D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339742_118339749dup , CM000673.2:g.118339742_118339749dup GRCh38
NC_000011.9:g.118210457_118210464dup , CM000673.1:g.118210457_118210464dup GRCh37
NC_000011.8:g.117715667_117715674dup NCBI36
NG_007566.1:g.399_406dup , LRG_39:g.399_406dup
NG_009891.1:g.8002_8009dup , LRG_37:g.8002_8009dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.925_932dup
ENST00000695667.1:n.443_450dup
ENST00000695668.1:n.2423_2430dup
ENST00000300692.9:c.406+32_406+39dup MANE Select ENSP00000300692.4:n.406+32_406+39dup
ENST00000300692.8:c.406+32_406+39dup ENSP00000300692.4:n.406+32_406+39dup
ENST00000392884.2:c.275-249_275-242dup ENSP00000376622.2:n.275-249_275-242dup
ENST00000526561.1:n.80-249_80-242dup
ENST00000529594.5:c.187+32_187+39dup ENSP00000437335.1:n.187+32_187+39dup
ENST00000534687.5:c.288-249_288-242dup
NM_000732.4:c.406+32_406+39dup , LRG_37t1:c.406+32_406+39dup NP_000723.1:n.406+32_406+39dup
NM_001040651.1:c.275-249_275-242dup NP_001035741.1:n.275-249_275-242dup
NM_001040651.2:c.275-249_275-242dup NP_001035741.1:n.275-249_275-242dup
NM_000732.6:c.406+32_406+39dup MANE Select NP_000723.1:n.406+32_406+39dup