Canonical Allele Identifier: CA382788256

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210556C>A (hg19) ; chr11:g.118339841C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339841C>A , CM000673.2:g.118339841C>A	GRCh38
NC_000011.9:g.118210556C>A , CM000673.1:g.118210556C>A	GRCh37
NC_000011.8:g.117715766C>A	NCBI36
NG_007566.1:g.498C>A , LRG_39:g.498C>A
NG_009891.1:g.7904G>T , LRG_37:g.7904G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.827G>T
ENST00000695667.1:n.345G>T
ENST00000695668.1:n.2325G>T
ENST00000300692.9:c.340G>T MANE Select	ENSP00000300692.4:p.Ala114Ser
ENST00000300692.8:c.340G>T	ENSP00000300692.4:p.Ala114Ser
ENST00000392884.2:c.275-347G>T	ENSP00000376622.2:n.275-347G>T
ENST00000526561.1:n.80-347G>T
ENST00000529594.5:c.121G>T	ENSP00000437335.1:p.Ala41Ser
ENST00000534687.5:c.288-347G>T
NM_000732.4:c.340G>T , LRG_37t1:c.340G>T	NP_000723.1:p.Ala114Ser
NM_001040651.1:c.275-347G>T	NP_001035741.1:n.275-347G>T
NM_001040651.2:c.275-347G>T	NP_001035741.1:n.275-347G>T
NM_000732.6:c.340G>T MANE Select	NP_000723.1:p.Ala114Ser