Canonical Allele Identifier: CA2215894897

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937795_28937796delinsTG , CM000678.2:g.28937795_28937796delinsTG	GRCh38
NC_000016.9:g.28949116_28949117delinsTG , CM000678.1:g.28949116_28949117delinsTG	GRCh37
NC_000016.8:g.28856617_28856618delinsTG	NCBI36
NG_007275.1:g.10857_10858delinsTG , LRG_35:g.10857_10858delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1456_1457delinsTG	ENSP00000313419.4:p.Trp486=
ENST00000538922.8:c.1456_1457delinsTG MANE Select	ENSP00000437940.2:p.Trp486=
ENST00000324662.7:c.1456_1457delinsTG	ENSP00000313419.3:p.Trp486=
ENST00000538922.5:c.1456_1457delinsTG	ENSP00000437940.1:p.Trp486=
ENST00000565089.5:n.1890_1891delinsTG
ENST00000567368.1:n.569+115_569+116delinsTG
ENST00000567541.5:c.1456_1457delinsTG	ENSP00000456201.1:p.Trp486=
ENST00000611258.4:c.*51_*52delinsTG	ENSP00000481090.1:n.*51_*52delinsTG
NM_001178098.1:c.1456_1457delinsTG	NP_001171569.1:p.Trp486=
NM_001770.5:c.1456_1457delinsTG , LRG_35t1:c.1456_1457delinsTG	NP_001761.3:p.Trp486=
XM_006721103.2:c.1189_1190delinsTG	XP_006721166.1:p.Trp397=
XM_006721103.3:c.1189_1190delinsTG	XP_006721166.1:p.Trp397=
XM_017023893.1:c.1189_1190delinsTG	XP_016879382.1:p.Trp397=
NM_001178098.2:c.1456_1457delinsTG	NP_001171569.1:p.Trp486=
NM_001770.6:c.1456_1457delinsTG MANE Select	NP_001761.3:p.Trp486=
NM_001385732.1:c.1189_1190delinsTG	NP_001372661.1:p.Trp397=
NR_169755.1:n.1798_1799delinsTG