Canonical Allele Identifier: CA7988381

Gene: CD19 RABEP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28933075C>G , CM000678.2:g.28933075C>G	GRCh38
NC_000016.9:g.28944396C>G , CM000678.1:g.28944396C>G	GRCh37
NC_000016.8:g.28851897C>G	NCBI36
NG_007275.1:g.6137C>G , LRG_35:g.6137C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001770.6:c.520C>G (CD19) MANE Select	NP_001761.3:p.Leu174Val
ENST00000538922.8:c.520C>G (CD19) MANE Select	ENSP00000437940.2:p.Leu174Val
NM_001178098.1:c.520C>G (CD19)	NP_001171569.1:p.Leu174Val
NM_001178098.2:c.520C>G (CD19)	NP_001171569.1:p.Leu174Val
NM_001385732.1:c.253C>G (CD19)	NP_001372661.1:p.Leu85Val
NM_001770.5:c.520C>G , LRG_35t1:c.520C>G (CD19)	NP_001761.3:p.Leu174Val
NR_169755.1:n.848C>G (CD19)
ENST00000324662.7:c.520C>G (CD19)	ENSP00000313419.3:p.Leu174Val
ENST00000324662.8:c.520C>G (CD19)	ENSP00000313419.4:p.Leu174Val
ENST00000538922.5:c.520C>G (CD19)	ENSP00000437940.1:p.Leu174Val
ENST00000565089.5:n.854C>G (CD19)
ENST00000566762.1:c.-150+3189G>C (RABEP2)	ENSP00000454974.1:n.-150+3189G>C
ENST00000566890.1:n.143C>G (CD19)
ENST00000567541.5:c.520C>G (CD19)	ENSP00000456201.1:p.Leu174Val
ENST00000611258.4:c.520C>G (CD19)	ENSP00000481090.1:p.Leu174Val
XM_006721103.2:c.253C>G (CD19)	XP_006721166.1:p.Leu85Val
XM_006721103.3:c.253C>G (CD19)	XP_006721166.1:p.Leu85Val
XM_011545981.1:c.520C>G (CD19)	XP_011544283.1:p.Leu174Val
XM_011545981.2:c.520C>G (CD19)	XP_011544283.1:p.Leu174Val
XM_017023893.1:c.253C>G (CD19)	XP_016879382.1:p.Leu85Val
XR_950871.1:n.582C>G (CD19)
XR_950871.2:n.565C>G (CD19)
XR_950872.1:n.582C>G (CD19)