Canonical Allele Identifier: CA6301848
Community Standard Title: NM_000732.6(CD3D):c.453C>T (p.Pro151=)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339225G>A , CM000673.2:g.118339225G>A GRCh38
NC_000011.9:g.118209940G>A , CM000673.1:g.118209940G>A GRCh37
NC_000011.8:g.117715150G>A NCBI36
NG_009891.1:g.8520C>T , LRG_37:g.8520C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.453C>T MANE Select NP_000723.1:p.Pro151=
ENST00000300692.9:c.453C>T MANE Select ENSP00000300692.4:p.Pro151=
NM_000732.4:c.453C>T , LRG_37t1:c.453C>T NP_000723.1:p.Pro151=
NM_001040651.1:c.321C>T NP_001035741.1:p.Pro107=
NM_001040651.2:c.321C>T NP_001035741.1:p.Pro107=
ENST00000300692.8:c.453C>T ENSP00000300692.4:p.Pro151=
ENST00000392884.2:c.321C>T ENSP00000376622.2:p.Pro107=
ENST00000526561.1:n.126C>T
ENST00000529594.5:c.234C>T ENSP00000437335.1:p.Pro78=
ENST00000534687.5:c.334C>T
ENST00000695666.1:n.1220C>T
ENST00000695667.1:n.738C>T