Canonical Allele Identifier: CA382794486
Community Standard Title: NM_000073.3(CD3G):c.484-1G>A
Gene: CD3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118352403G>A , CM000673.2:g.118352403G>A GRCh38
NC_000011.9:g.118223118G>A , CM000673.1:g.118223118G>A GRCh37
NC_000011.8:g.117728328G>A NCBI36
NG_007566.1:g.13060G>A , LRG_39:g.13060G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000073.3:c.484-1G>A MANE Select NP_000064.1:n.484-1G>A
ENST00000532917.3:c.484-1G>A MANE Select ENSP00000431445.2:n.484-1G>A
NM_000073.2:c.484-1G>A , LRG_39t1:c.484-1G>A NP_000064.1:n.484-1G>A
ENST00000292144.8:c.*541-1G>A ENSP00000292144.4:n.*541-1G>A
ENST00000392883.6:c.172-1G>A ENSP00000376621.2:n.172-1G>A
ENST00000532903.1:n.560-1G>A
ENST00000532917.1:c.484-1G>A ENSP00000431445.1:n.484-1G>A
XM_006718941.2:c.484-1G>A XP_006719004.1:n.484-1G>A
XM_006718941.3:c.484-1G>A XP_006719004.1:n.484-1G>A