Canonical Allele Identifier: CA2338111223
Gene: CBLC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793770_44793772delinsGTC , CM000681.2:g.44793770_44793772delinsGTC GRCh38
NC_000019.9:g.45297027_45297029delinsGTC , CM000681.1:g.45297027_45297029delinsGTC GRCh37
NC_000019.8:g.49988867_49988869delinsGTC NCBI36
NG_054718.1:g.20916_20918delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647358.2:c.1284+150_1284+152delinsGTC MANE Select ENSP00000494162.1:n.1284+150_1284+152delinsGTC
ENST00000270279.7:c.1284+150_1284+152delinsGTC ENSP00000270279.3:n.1284+150_1284+152delinsGTC
ENST00000341505.4:c.1146+150_1146+152delinsGTC ENSP00000340250.4:n.1146+150_1146+152delinsGTC
NM_001130852.1:c.1146+150_1146+152delinsGTC NP_001124324.1:n.1146+150_1146+152delinsGTC
NM_012116.3:c.1284+150_1284+152delinsGTC NP_036248.3:n.1284+150_1284+152delinsGTC
XM_005258696.2:c.1284+150_1284+152delinsGTC XP_005258753.1:n.1284+150_1284+152delinsGTC
XM_011526688.1:c.1284+150_1284+152delinsGTC XP_011524990.1:n.1284+150_1284+152delinsGTC
XM_011526689.1:c.1146+150_1146+152delinsGTC XP_011524991.1:n.1146+150_1146+152delinsGTC
XR_935783.1:n.1231+150_1231+152delinsGTC
NM_012116.4:c.1284+150_1284+152delinsGTC MANE Select NP_036248.3:n.1284+150_1284+152delinsGTC
XM_005258696.3:c.1284+150_1284+152delinsGTC XP_005258753.1:n.1284+150_1284+152delinsGTC
XM_011526688.2:c.1284+150_1284+152delinsGTC XP_011524990.1:n.1284+150_1284+152delinsGTC
XM_011526689.2:c.1146+150_1146+152delinsGTC XP_011524991.1:n.1146+150_1146+152delinsGTC
XR_935783.2:n.1236+150_1236+152delinsGTC