Canonical Allele Identifier: CA2338111181
Gene: CBLC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793697_44793769delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA , CM000681.2:g.44793697_44793769delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA GRCh38
NC_000019.9:g.45296954_45297026delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA , CM000681.1:g.45296954_45297026delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA GRCh37
NC_000019.8:g.49988794_49988866delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA NCBI36
NG_054718.1:g.20843_20915delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647358.2:c.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA MANE Select ENSP00000494162.1:n.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGAC...
ENST00000270279.7:c.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA ENSP00000270279.3:n.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGAC...
ENST00000341505.4:c.1146+77_1146+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA ENSP00000340250.4:n.1146+77_1146+149delinsGGTCTGAGGGAGGAGAGAC...
NM_001130852.1:c.1146+77_1146+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA NP_001124324.1:n.1146+77_1146+149delinsGGTCTGAGGGAGGAGAGACTGG...
NM_012116.3:c.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA NP_036248.3:n.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGG...
XM_005258696.2:c.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA XP_005258753.1:n.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGG...
XM_011526688.1:c.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA XP_011524990.1:n.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGG...
XM_011526689.1:c.1146+77_1146+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA XP_011524991.1:n.1146+77_1146+149delinsGGTCTGAGGGAGGAGAGACTGG...
XR_935783.1:n.1231+77_1231+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA
NM_012116.4:c.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA MANE Select NP_036248.3:n.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGG...
XM_005258696.3:c.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA XP_005258753.1:n.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGG...
XM_011526688.2:c.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA XP_011524990.1:n.1284+77_1284+149delinsGGTCTGAGGGAGGAGAGACTGG...
XM_011526689.2:c.1146+77_1146+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA XP_011524991.1:n.1146+77_1146+149delinsGGTCTGAGGGAGGAGAGACTGG...
XR_935783.2:n.1236+77_1236+149delinsGGTCTGAGGGAGGAGAGACTGGGGGCCTGGACTCCTGGGTCTGAGGGAAGAGGGGTTGGAGCCTGTACTCTGA