Canonical Allele Identifier: CA1976823665

Gene: MS4A7 MS4A14 MS4A6E

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.60387527T= , CM000673.2:g.60387527T=	GRCh38
NC_000011.9:g.60155000T= , CM000673.1:g.60155000T=	GRCh37
NC_000011.8:g.59911576T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021201.5:c.339+754T= (MS4A7) MANE Select	NP_067024.1:n.339+754T=
ENST00000300184.8:c.339+754T= (MS4A7) MANE Select	ENSP00000300184.3:n.339+754T=
NM_021201.4:c.339+754T= (MS4A7)	NP_067024.1:n.339+754T=
NM_206938.1:c.204+754T= (MS4A7)	NP_996821.1:n.204+754T=
NM_206938.2:c.204+754T= (MS4A7)	NP_996821.1:n.204+754T=
NM_206939.1:c.339+754T= (MS4A7)	NP_996822.1:n.339+754T=
NM_206939.2:c.339+754T= (MS4A7)	NP_996822.1:n.339+754T=
NM_206940.1:c.204+754T= (MS4A7)	NP_996823.1:n.204+754T=
NM_206940.2:c.204+754T= (MS4A7)	NP_996823.1:n.204+754T=
ENST00000300184.7:c.339+754T= (MS4A7)	ENSP00000300184.3:n.339+754T=
ENST00000358246.5:c.204+754T= (MS4A7)	ENSP00000350983.1:n.204+754T=
ENST00000528808.1:n.350+754T= (MS4A7)
ENST00000530027.5:c.148-1863T= (MS4A7)	ENSP00000434819.1:n.148-1863T=
ENST00000530234.2:c.282+2305T= (MS4A7)	ENSP00000433184.1:n.282+2305T=
ENST00000530614.5:c.204+754T= (MS4A7)	ENSP00000433861.1:n.204+754T=
ENST00000531787.5:c.-19+8863T= (MS4A14)	ENSP00000437222.1:n.-19+8863T=
ENST00000532756.1:c.532-9035T= (MS4A6E)	ENSP00000432963.1:n.532-9035T=
ENST00000534016.5:c.204+754T= (MS4A7)	ENSP00000434637.1:n.204+754T=
ENST00000534310.5:n.274+754T= (MS4A7)