Canonical Allele Identifier: CA2338111104
Gene: CBLC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793540T= , CM000681.2:g.44793540T= GRCh38
NC_000019.9:g.45296797T= , CM000681.1:g.45296797T= GRCh37
NC_000019.8:g.49988637T= NCBI36
NG_054718.1:g.20686T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647358.2:c.1204T= MANE Select ENSP00000494162.1:p.Tyr402=
ENST00000270279.7:c.1204T= ENSP00000270279.3:p.Tyr402=
ENST00000341505.4:c.1066T= ENSP00000340250.4:p.Tyr356=
NM_001130852.1:c.1066T= NP_001124324.1:p.Tyr356=
NM_012116.3:c.1204T= NP_036248.3:p.Tyr402=
XM_005258696.2:c.1204T= XP_005258753.1:p.Tyr402=
XM_011526688.1:c.1204T= XP_011524990.1:p.Tyr402=
XM_011526689.1:c.1066T= XP_011524991.1:p.Tyr356=
XR_935783.1:n.1151T=
NM_012116.4:c.1204T= MANE Select NP_036248.3:p.Tyr402=
XM_005258696.3:c.1204T= XP_005258753.1:p.Tyr402=
XM_011526688.2:c.1204T= XP_011524990.1:p.Tyr402=
XM_011526689.2:c.1066T= XP_011524991.1:p.Tyr356=
XR_935783.2:n.1156T=