Canonical Allele Identifier: CA996238544
Gene: CBLC HGNC NCBI

Linked Data

dbSNP Id: rs1968114121

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793711_44793781del , CM000681.2:g.44793711_44793781del GRCh38
NC_000019.9:g.45296968_45297038del , CM000681.1:g.45296968_45297038del GRCh37
NC_000019.8:g.49988808_49988878del NCBI36
NG_054718.1:g.20857_20927del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647358.2:c.1284+91_1284+161del MANE Select ENSP00000494162.1:n.1284+91_1284+161del
ENST00000270279.7:c.1284+91_1284+161del ENSP00000270279.3:n.1284+91_1284+161del
ENST00000341505.4:c.1146+91_1146+161del ENSP00000340250.4:n.1146+91_1146+161del
NM_001130852.1:c.1146+91_1146+161del NP_001124324.1:n.1146+91_1146+161del
NM_012116.3:c.1284+91_1284+161del NP_036248.3:n.1284+91_1284+161del
XM_005258696.2:c.1284+91_1284+161del XP_005258753.1:n.1284+91_1284+161del
XM_011526688.1:c.1284+91_1284+161del XP_011524990.1:n.1284+91_1284+161del
XM_011526689.1:c.1146+91_1146+161del XP_011524991.1:n.1146+91_1146+161del
XR_935783.1:n.1231+91_1231+161del
NM_012116.4:c.1284+91_1284+161del MANE Select NP_036248.3:n.1284+91_1284+161del
XM_005258696.3:c.1284+91_1284+161del XP_005258753.1:n.1284+91_1284+161del
XM_011526688.2:c.1284+91_1284+161del XP_011524990.1:n.1284+91_1284+161del
XM_011526689.2:c.1146+91_1146+161del XP_011524991.1:n.1146+91_1146+161del
XR_935783.2:n.1236+91_1236+161del