Canonical Allele Identifier: CA382788499

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210620C>A (hg19) ; chr11:g.118339905C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339905C>A , CM000673.2:g.118339905C>A	GRCh38
NC_000011.9:g.118210620C>A , CM000673.1:g.118210620C>A	GRCh37
NC_000011.8:g.117715830C>A	NCBI36
NG_007566.1:g.562C>A , LRG_39:g.562C>A
NG_009891.1:g.7840G>T , LRG_37:g.7840G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695666.1:n.763G>T
ENST00000695667.1:n.281G>T
ENST00000695668.1:n.2261G>T
ENST00000300692.9:c.276G>T MANE Select	ENSP00000300692.4:p.Met92Ile
ENST00000300692.8:c.276G>T	ENSP00000300692.4:p.Met92Ile
ENST00000392884.2:c.275-411G>T	ENSP00000376622.2:n.275-411G>T
ENST00000526561.1:n.80-411G>T
ENST00000529594.5:c.57G>T	ENSP00000437335.1:p.Val19=
ENST00000534687.5:c.288-411G>T
NM_000732.4:c.276G>T , LRG_37t1:c.276G>T	NP_000723.1:p.Met92Ile
NM_001040651.1:c.275-411G>T	NP_001035741.1:n.275-411G>T
NM_001040651.2:c.275-411G>T	NP_001035741.1:n.275-411G>T
NM_000732.6:c.276G>T MANE Select	NP_000723.1:p.Met92Ile