Canonical Allele Identifier: CA2616232378

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339654-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339654C>G , CM000673.2:g.118339654C>G	GRCh38
NC_000011.9:g.118210369C>G , CM000673.1:g.118210369C>G	GRCh37
NC_000011.8:g.117715579C>G	NCBI36
NG_007566.1:g.311C>G , LRG_39:g.311C>G
NG_009891.1:g.8091G>C , LRG_37:g.8091G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.1014G>C
ENST00000695667.1:n.532G>C
ENST00000300692.9:c.406+121G>C MANE Select	ENSP00000300692.4:n.406+121G>C
ENST00000300692.8:c.406+121G>C	ENSP00000300692.4:n.406+121G>C
ENST00000392884.2:c.275-160G>C	ENSP00000376622.2:n.275-160G>C
ENST00000526561.1:n.80-160G>C
ENST00000529594.5:c.187+121G>C	ENSP00000437335.1:n.187+121G>C
ENST00000534687.5:c.288-160G>C
NM_000732.4:c.406+121G>C , LRG_37t1:c.406+121G>C	NP_000723.1:n.406+121G>C
NM_001040651.1:c.275-160G>C	NP_001035741.1:n.275-160G>C
NM_001040651.2:c.275-160G>C	NP_001035741.1:n.275-160G>C
NM_000732.6:c.406+121G>C MANE Select	NP_000723.1:n.406+121G>C