Canonical Allele Identifier: CA2338111233
Gene: CBLC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793793_44793868delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC , CM000681.2:g.44793793_44793868delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC GRCh38
NC_000019.9:g.45297050_45297125delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC , CM000681.1:g.45297050_45297125delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC GRCh37
NC_000019.8:g.49988890_49988965delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC NCBI36
NG_054718.1:g.20939_21014delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647358.2:c.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC MANE Select ENSP00000494162.1:n.1284+173_1284+248delinsTCCTGGACTCCTGGGTCT...
ENST00000270279.7:c.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC ENSP00000270279.3:n.1284+173_1284+248delinsTCCTGGACTCCTGGGTCT...
ENST00000341505.4:c.1146+173_1146+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC ENSP00000340250.4:n.1146+173_1146+248delinsTCCTGGACTCCTGGGTCT...
NM_001130852.1:c.1146+173_1146+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC NP_001124324.1:n.1146+173_1146+248delinsTCCTGGACTCCTGGGTCTGAG...
NM_012116.3:c.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC NP_036248.3:n.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAGGGA...
XM_005258696.2:c.1284+173_1285-239delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC XP_005258753.1:n.1284+173_1285-239delinsTCCTGGACTCCTGGGTCTGAG...
XM_011526688.1:c.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC XP_011524990.1:n.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAG...
XM_011526689.1:c.1146+173_1146+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC XP_011524991.1:n.1146+173_1146+248delinsTCCTGGACTCCTGGGTCTGAG...
XR_935783.1:n.1231+173_1231+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC
NM_012116.4:c.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC MANE Select NP_036248.3:n.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAGGGA...
XM_005258696.3:c.1284+173_1285-239delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC XP_005258753.1:n.1284+173_1285-239delinsTCCTGGACTCCTGGGTCTGAG...
XM_011526688.2:c.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC XP_011524990.1:n.1284+173_1284+248delinsTCCTGGACTCCTGGGTCTGAG...
XM_011526689.2:c.1146+173_1146+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC XP_011524991.1:n.1146+173_1146+248delinsTCCTGGACTCCTGGGTCTGAG...
XR_935783.2:n.1236+173_1236+248delinsTCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTAGGGGCCTGGACTCCTGGGTCTGATGGAGGTGGGTATGGGGAC