Canonical Allele Identifier: CA2499903636
Gene: CBLC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793719_44793722del , CM000681.2:g.44793719_44793722del GRCh38
NC_000019.9:g.45296976_45296979del , CM000681.1:g.45296976_45296979del GRCh37
NC_000019.8:g.49988816_49988819del NCBI36
NG_054718.1:g.20865_20868del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647358.2:c.1284+99_1284+102del MANE Select ENSP00000494162.1:n.1284+99_1284+102del
ENST00000270279.7:c.1284+99_1284+102del ENSP00000270279.3:n.1284+99_1284+102del
ENST00000341505.4:c.1146+99_1146+102del ENSP00000340250.4:n.1146+99_1146+102del
NM_001130852.1:c.1146+99_1146+102del NP_001124324.1:n.1146+99_1146+102del
NM_012116.3:c.1284+99_1284+102del NP_036248.3:n.1284+99_1284+102del
XM_005258696.2:c.1284+99_1284+102del XP_005258753.1:n.1284+99_1284+102del
XM_011526688.1:c.1284+99_1284+102del XP_011524990.1:n.1284+99_1284+102del
XM_011526689.1:c.1146+99_1146+102del XP_011524991.1:n.1146+99_1146+102del
XR_935783.1:n.1231+99_1231+102del
NM_012116.4:c.1284+99_1284+102del MANE Select NP_036248.3:n.1284+99_1284+102del
XM_005258696.3:c.1284+99_1284+102del XP_005258753.1:n.1284+99_1284+102del
XM_011526688.2:c.1284+99_1284+102del XP_011524990.1:n.1284+99_1284+102del
XM_011526689.2:c.1146+99_1146+102del XP_011524991.1:n.1146+99_1146+102del
XR_935783.2:n.1236+99_1236+102del