Canonical Allele Identifier: CA2814530696
Gene: CBLC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793714_44793715insAT , CM000681.2:g.44793714_44793715insAT GRCh38
NC_000019.9:g.45296971_45296972insAT , CM000681.1:g.45296971_45296972insAT GRCh37
NC_000019.8:g.49988811_49988812insAT NCBI36
NG_054718.1:g.20860_20861insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647358.2:c.1284+94_1284+95insAT MANE Select ENSP00000494162.1:n.1284+94_1284+95insAT
ENST00000270279.7:c.1284+94_1284+95insAT ENSP00000270279.3:n.1284+94_1284+95insAT
ENST00000341505.4:c.1146+94_1146+95insAT ENSP00000340250.4:n.1146+94_1146+95insAT
NM_001130852.1:c.1146+94_1146+95insAT NP_001124324.1:n.1146+94_1146+95insAT
NM_012116.3:c.1284+94_1284+95insAT NP_036248.3:n.1284+94_1284+95insAT
XM_005258696.2:c.1284+94_1284+95insAT XP_005258753.1:n.1284+94_1284+95insAT
XM_011526688.1:c.1284+94_1284+95insAT XP_011524990.1:n.1284+94_1284+95insAT
XM_011526689.1:c.1146+94_1146+95insAT XP_011524991.1:n.1146+94_1146+95insAT
XR_935783.1:n.1231+94_1231+95insAT
NM_012116.4:c.1284+94_1284+95insAT MANE Select NP_036248.3:n.1284+94_1284+95insAT
XM_005258696.3:c.1284+94_1284+95insAT XP_005258753.1:n.1284+94_1284+95insAT
XM_011526688.2:c.1284+94_1284+95insAT XP_011524990.1:n.1284+94_1284+95insAT
XM_011526689.2:c.1146+94_1146+95insAT XP_011524991.1:n.1146+94_1146+95insAT
XR_935783.2:n.1236+94_1236+95insAT