Canonical Allele Identifier: CA996238541

Gene: CBLC

Linked Data

• dbSNP Id: rs1968114055
• gnomAD v3: 19-44793710-AGAGACTGGGGGCCTGGACTCCTGGGTCTG-A
• gnomAD v4: 19-44793710-AGAGACTGGGGGCCTGGACTCCTGGGTCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44793711_44793739del , CM000681.2:g.44793711_44793739del	GRCh38
NC_000019.9:g.45296968_45296996del , CM000681.1:g.45296968_45296996del	GRCh37
NC_000019.8:g.49988808_49988836del	NCBI36
NG_054718.1:g.20857_20885del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647358.2:c.1284+91_1284+119del MANE Select	ENSP00000494162.1:n.1284+91_1284+119del
ENST00000270279.7:c.1284+91_1284+119del	ENSP00000270279.3:n.1284+91_1284+119del
ENST00000341505.4:c.1146+91_1146+119del	ENSP00000340250.4:n.1146+91_1146+119del
NM_001130852.1:c.1146+91_1146+119del	NP_001124324.1:n.1146+91_1146+119del
NM_012116.3:c.1284+91_1284+119del	NP_036248.3:n.1284+91_1284+119del
XM_005258696.2:c.1284+91_1284+119del	XP_005258753.1:n.1284+91_1284+119del
XM_011526688.1:c.1284+91_1284+119del	XP_011524990.1:n.1284+91_1284+119del
XM_011526689.1:c.1146+91_1146+119del	XP_011524991.1:n.1146+91_1146+119del
XR_935783.1:n.1231+91_1231+119del
NM_012116.4:c.1284+91_1284+119del MANE Select	NP_036248.3:n.1284+91_1284+119del
XM_005258696.3:c.1284+91_1284+119del	XP_005258753.1:n.1284+91_1284+119del
XM_011526688.2:c.1284+91_1284+119del	XP_011524990.1:n.1284+91_1284+119del
XM_011526689.2:c.1146+91_1146+119del	XP_011524991.1:n.1146+91_1146+119del
XR_935783.2:n.1236+91_1236+119del