Canonical Allele Identifier: CA1140064248

Gene: CD84

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160546518A= , CM000663.2:g.160546518A=	GRCh38
NC_000001.10:g.160516308A= , CM000663.1:g.160516308A=	GRCh37
NC_000001.9:g.158782932A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368054.8:c.*1738T= MANE Select	ENSP00000357033.4:n.*1738T=
ENST00000368054.7:c.*1738T=	ENSP00000357033.3:n.*1738T=
ENST00000534968.5:c.*1738T=	ENSP00000442845.1:n.*1738T=
NM_001184879.1:c.*1738T=	NP_001171808.1:n.*1738T=
NM_001184881.1:c.*1808T=	NP_001171810.1:n.*1808T=
NM_001184882.1:c.*1738T=	NP_001171811.1:n.*1738T=
NM_003874.3:c.*1738T=	NP_003865.1:n.*1738T=
XM_011510094.1:c.*1738T=	XP_011508396.1:n.*1738T=
XM_011510095.1:c.*1738T=	XP_011508397.1:n.*1738T=
XR_922203.1:n.611+9331A=
NM_001330742.1:c.*1738T=	NP_001317671.1:n.*1738T=
XM_011510095.2:c.*1738T=	XP_011508397.1:n.*1738T=
XR_002957960.1:n.5453T=
XR_922203.2:n.1541+9331A=
NM_001184879.2:c.*1738T=	NP_001171808.1:n.*1738T=
NM_001184881.2:c.*1808T=	NP_001171810.1:n.*1808T=
NM_001330742.2:c.*1738T=	NP_001317671.1:n.*1738T=
NM_003874.4:c.*1738T= MANE Select	NP_003865.1:n.*1738T=
NM_001184882.2:c.*1738T=	NP_001171811.1:n.*1738T=