Canonical Allele Identifier: CA507795849

Gene: CBLC

Linked Data

• COSMIC: COSM3960196
• MyVariant Identifiers: chr19:g.45296820T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44793563T>A , CM000681.2:g.44793563T>A	GRCh38
NC_000019.9:g.45296820T>A , CM000681.1:g.45296820T>A	GRCh37
NC_000019.8:g.49988660T>A	NCBI36
NG_054718.1:g.20709T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647358.2:c.1227T>A MANE Select	ENSP00000494162.1:p.Thr409=
ENST00000270279.7:c.1227T>A	ENSP00000270279.3:p.Thr409=
ENST00000341505.4:c.1089T>A	ENSP00000340250.4:p.Thr363=
NM_001130852.1:c.1089T>A	NP_001124324.1:p.Thr363=
NM_012116.3:c.1227T>A	NP_036248.3:p.Thr409=
XM_005258696.2:c.1227T>A	XP_005258753.1:p.Thr409=
XM_011526688.1:c.1227T>A	XP_011524990.1:p.Thr409=
XM_011526689.1:c.1089T>A	XP_011524991.1:p.Thr363=
XR_935783.1:n.1174T>A
NM_012116.4:c.1227T>A MANE Select	NP_036248.3:p.Thr409=
XM_005258696.3:c.1227T>A	XP_005258753.1:p.Thr409=
XM_011526688.2:c.1227T>A	XP_011524990.1:p.Thr409=
XM_011526689.2:c.1089T>A	XP_011524991.1:p.Thr363=
XR_935783.2:n.1179T>A