Canonical Allele Identifier: CA2215894645

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937274_28937277delinsCAGA , CM000678.2:g.28937274_28937277delinsCAGA	GRCh38
NC_000016.9:g.28948595_28948598delinsCAGA , CM000678.1:g.28948595_28948598delinsCAGA	GRCh37
NC_000016.8:g.28856096_28856099delinsCAGA	NCBI36
NG_007275.1:g.10336_10339delinsCAGA , LRG_35:g.10336_10339delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1202_1205delinsCAGA	ENSP00000313419.4:p.Pro401=
ENST00000538922.8:c.1202_1205delinsCAGA MANE Select	ENSP00000437940.2:p.Pro401=
ENST00000324662.7:c.1202_1205delinsCAGA	ENSP00000313419.3:p.Pro401=
ENST00000538922.5:c.1202_1205delinsCAGA	ENSP00000437940.1:p.Pro401=
ENST00000565089.5:n.1536_1539delinsCAGA
ENST00000567368.1:n.342_345delinsCAGA
ENST00000567541.5:c.1202_1205delinsCAGA	ENSP00000456201.1:p.Pro401=
ENST00000611258.4:c.1201_1204delinsCAGA	ENSP00000481090.1:p.Gln401=
NM_001178098.1:c.1202_1205delinsCAGA	NP_001171569.1:p.Pro401=
NM_001770.5:c.1202_1205delinsCAGA , LRG_35t1:c.1202_1205delinsCAGA	NP_001761.3:p.Pro401=
XM_006721103.2:c.935_938delinsCAGA	XP_006721166.1:p.Pro312=
XM_006721103.3:c.935_938delinsCAGA	XP_006721166.1:p.Pro312=
XM_017023893.1:c.935_938delinsCAGA	XP_016879382.1:p.Pro312=
NM_001178098.2:c.1202_1205delinsCAGA	NP_001171569.1:p.Pro401=
NM_001770.6:c.1202_1205delinsCAGA MANE Select	NP_001761.3:p.Pro401=
NM_001385732.1:c.935_938delinsCAGA	NP_001372661.1:p.Pro312=
NR_169755.1:n.1544_1547delinsCAGA