Canonical Allele Identifier: CA2585699099
Gene: CBLC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793685_44793686insTGGGGT , CM000681.2:g.44793685_44793686insTGGGGT GRCh38
NC_000019.9:g.45296942_45296943insTGGGGT , CM000681.1:g.45296942_45296943insTGGGGT GRCh37
NC_000019.8:g.49988782_49988783insTGGGGT NCBI36
NG_054718.1:g.20831_20832insTGGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647358.2:c.1284+65_1284+66insTGGGGT MANE Select ENSP00000494162.1:n.1284+65_1284+66insTGGGGT
ENST00000270279.7:c.1284+65_1284+66insTGGGGT ENSP00000270279.3:n.1284+65_1284+66insTGGGGT
ENST00000341505.4:c.1146+65_1146+66insTGGGGT ENSP00000340250.4:n.1146+65_1146+66insTGGGGT
NM_001130852.1:c.1146+65_1146+66insTGGGGT NP_001124324.1:n.1146+65_1146+66insTGGGGT
NM_012116.3:c.1284+65_1284+66insTGGGGT NP_036248.3:n.1284+65_1284+66insTGGGGT
XM_005258696.2:c.1284+65_1284+66insTGGGGT XP_005258753.1:n.1284+65_1284+66insTGGGGT
XM_011526688.1:c.1284+65_1284+66insTGGGGT XP_011524990.1:n.1284+65_1284+66insTGGGGT
XM_011526689.1:c.1146+65_1146+66insTGGGGT XP_011524991.1:n.1146+65_1146+66insTGGGGT
XR_935783.1:n.1231+65_1231+66insTGGGGT
NM_012116.4:c.1284+65_1284+66insTGGGGT MANE Select NP_036248.3:n.1284+65_1284+66insTGGGGT
XM_005258696.3:c.1284+65_1284+66insTGGGGT XP_005258753.1:n.1284+65_1284+66insTGGGGT
XM_011526688.2:c.1284+65_1284+66insTGGGGT XP_011524990.1:n.1284+65_1284+66insTGGGGT
XM_011526689.2:c.1146+65_1146+66insTGGGGT XP_011524991.1:n.1146+65_1146+66insTGGGGT
XR_935783.2:n.1236+65_1236+66insTGGGGT