Canonical Allele Identifier: CA2215894676

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937341_28937342delinsCG , CM000678.2:g.28937341_28937342delinsCG	GRCh38
NC_000016.9:g.28948662_28948663delinsCG , CM000678.1:g.28948662_28948663delinsCG	GRCh37
NC_000016.8:g.28856163_28856164delinsCG	NCBI36
NG_007275.1:g.10403_10404delinsCG , LRG_35:g.10403_10404delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1269_1270delinsCG	ENSP00000313419.4:p.Asn423=
ENST00000538922.8:c.1269_1270delinsCG MANE Select	ENSP00000437940.2:p.Asn423=
ENST00000324662.7:c.1269_1270delinsCG	ENSP00000313419.3:p.Asn423=
ENST00000538922.5:c.1269_1270delinsCG	ENSP00000437940.1:p.Asn423=
ENST00000565089.5:n.1603_1604delinsCG
ENST00000567368.1:n.409_410delinsCG
ENST00000567541.5:c.1269_1270delinsCG	ENSP00000456201.1:p.Asn423=
ENST00000611258.4:c.1268_1269delinsCG	ENSP00000481090.1:p.Thr423=
NM_001178098.1:c.1269_1270delinsCG	NP_001171569.1:p.Asn423=
NM_001770.5:c.1269_1270delinsCG , LRG_35t1:c.1269_1270delinsCG	NP_001761.3:p.Asn423=
XM_006721103.2:c.1002_1003delinsCG	XP_006721166.1:p.Asn334=
XM_006721103.3:c.1002_1003delinsCG	XP_006721166.1:p.Asn334=
XM_017023893.1:c.1002_1003delinsCG	XP_016879382.1:p.Asn334=
NM_001178098.2:c.1269_1270delinsCG	NP_001171569.1:p.Asn423=
NM_001770.6:c.1269_1270delinsCG MANE Select	NP_001761.3:p.Asn423=
NM_001385732.1:c.1002_1003delinsCG	NP_001372661.1:p.Asn334=
NR_169755.1:n.1611_1612delinsCG