Canonical Allele Identifier: CA477087181
Community Standard Title: NM_000732.6(CD3D):c.411C>A (p.Ala137=)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339490G>T , CM000673.2:g.118339490G>T GRCh38
NC_000011.9:g.118210205G>T , CM000673.1:g.118210205G>T GRCh37
NC_000011.8:g.117715415G>T NCBI36
NG_007566.1:g.147G>T , LRG_39:g.147G>T
NG_009891.1:g.8255C>A , LRG_37:g.8255C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.411C>A MANE Select NP_000723.1:p.Ala137=
ENST00000300692.9:c.411C>A MANE Select ENSP00000300692.4:p.Ala137=
NM_000732.4:c.411C>A , LRG_37t1:c.411C>A NP_000723.1:p.Ala137=
NM_001040651.1:c.279C>A NP_001035741.1:p.Ala93=
NM_001040651.2:c.279C>A NP_001035741.1:p.Ala93=
ENST00000300692.8:c.411C>A ENSP00000300692.4:p.Ala137=
ENST00000392884.2:c.279C>A ENSP00000376622.2:p.Ala93=
ENST00000526561.1:n.84C>A
ENST00000529594.5:c.192C>A ENSP00000437335.1:p.Ala64=
ENST00000534687.5:c.292C>A
ENST00000695666.1:n.1178C>A
ENST00000695667.1:n.696C>A