Canonical Allele Identifier: CA2616232392

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339681-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339681T>G , CM000673.2:g.118339681T>G	GRCh38
NC_000011.9:g.118210396T>G , CM000673.1:g.118210396T>G	GRCh37
NC_000011.8:g.117715606T>G	NCBI36
NG_007566.1:g.338T>G , LRG_39:g.338T>G
NG_009891.1:g.8064A>C , LRG_37:g.8064A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.987A>C
ENST00000695667.1:n.505A>C
ENST00000300692.9:c.406+94A>C MANE Select	ENSP00000300692.4:n.406+94A>C
ENST00000300692.8:c.406+94A>C	ENSP00000300692.4:n.406+94A>C
ENST00000392884.2:c.275-187A>C	ENSP00000376622.2:n.275-187A>C
ENST00000526561.1:n.80-187A>C
ENST00000529594.5:c.187+94A>C	ENSP00000437335.1:n.187+94A>C
ENST00000534687.5:c.288-187A>C
NM_000732.4:c.406+94A>C , LRG_37t1:c.406+94A>C	NP_000723.1:n.406+94A>C
NM_001040651.1:c.275-187A>C	NP_001035741.1:n.275-187A>C
NM_001040651.2:c.275-187A>C	NP_001035741.1:n.275-187A>C
NM_000732.6:c.406+94A>C MANE Select	NP_000723.1:n.406+94A>C