Canonical Allele Identifier: CA882679749

Gene: CBLC

Linked Data

• dbSNP Id: rs1247396063
• gnomAD v3: 19-44793770-GTC-G
• gnomAD v4: 19-44793770-GTC-G
• MyVariant Identifiers: chr19:g.45297028_45297029del (hg19) ; chr19:g.44793771_44793772del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44793772_44793773del , CM000681.2:g.44793772_44793773del	GRCh38
NC_000019.9:g.45297029_45297030del , CM000681.1:g.45297029_45297030del	GRCh37
NC_000019.8:g.49988869_49988870del	NCBI36
NG_054718.1:g.20918_20919del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647358.2:c.1284+152_1284+153del MANE Select	ENSP00000494162.1:n.1284+152_1284+153del
ENST00000270279.7:c.1284+152_1284+153del	ENSP00000270279.3:n.1284+152_1284+153del
ENST00000341505.4:c.1146+152_1146+153del	ENSP00000340250.4:n.1146+152_1146+153del
NM_001130852.1:c.1146+152_1146+153del	NP_001124324.1:n.1146+152_1146+153del
NM_012116.3:c.1284+152_1284+153del	NP_036248.3:n.1284+152_1284+153del
XM_005258696.2:c.1284+152_1284+153del	XP_005258753.1:n.1284+152_1284+153del
XM_011526688.1:c.1284+152_1284+153del	XP_011524990.1:n.1284+152_1284+153del
XM_011526689.1:c.1146+152_1146+153del	XP_011524991.1:n.1146+152_1146+153del
XR_935783.1:n.1231+152_1231+153del
NM_012116.4:c.1284+152_1284+153del MANE Select	NP_036248.3:n.1284+152_1284+153del
XM_005258696.3:c.1284+152_1284+153del	XP_005258753.1:n.1284+152_1284+153del
XM_011526688.2:c.1284+152_1284+153del	XP_011524990.1:n.1284+152_1284+153del
XM_011526689.2:c.1146+152_1146+153del	XP_011524991.1:n.1146+152_1146+153del
XR_935783.2:n.1236+152_1236+153del