Canonical Allele Identifier: CA2474800687

Gene: TRABD2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.47917976_47917978delinsAAC , CM000663.2:g.47917976_47917978delinsAAC	GRCh38
NC_000001.10:g.48383648_48383650delinsAAC , CM000663.1:g.48383648_48383650delinsAAC	GRCh37
NC_000001.9:g.48156235_48156237delinsAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606738.3:c.666+76056_666+76058delinsGTT MANE Select	ENSP00000476820.1:n.666+76056_666+76058delinsGTT
ENST00000435576.2:n.179+76056_179+76058delinsGTT
ENST00000606738.2:c.666+76056_666+76058delinsGTT	ENSP00000476820.1:n.666+76056_666+76058delinsGTT
NM_001194986.1:c.666+76056_666+76058delinsGTT	NP_001181915.1:n.666+76056_666+76058delinsGTT
XM_006710640.2:c.666+76056_666+76058delinsGTT	XP_006710703.1:n.666+76056_666+76058delinsGTT
XM_011541442.1:c.666+76056_666+76058delinsGTT	XP_011539744.1:n.666+76056_666+76058delinsGTT
XM_011541443.1:c.666+76056_666+76058delinsGTT	XP_011539745.1:n.666+76056_666+76058delinsGTT
XM_011541444.1:c.666+76056_666+76058delinsGTT	XP_011539746.1:n.666+76056_666+76058delinsGTT
XM_011541445.1:c.666+76056_666+76058delinsGTT	XP_011539747.1:n.666+76056_666+76058delinsGTT
XR_426606.2:n.1246+76056_1246+76058delinsGTT
XR_946653.1:n.1247+76056_1247+76058delinsGTT
XR_946654.1:n.1247+76056_1247+76058delinsGTT
XM_006710640.4:c.666+76056_666+76058delinsGTT	XP_006710703.1:n.666+76056_666+76058delinsGTT
XM_011541443.3:c.666+76056_666+76058delinsGTT	XP_011539745.1:n.666+76056_666+76058delinsGTT
XM_011541444.2:c.666+76056_666+76058delinsGTT	XP_011539746.1:n.666+76056_666+76058delinsGTT
XM_011541445.3:c.666+76056_666+76058delinsGTT	XP_011539747.1:n.666+76056_666+76058delinsGTT
XM_017001260.2:c.666+76056_666+76058delinsGTT	XP_016856749.1:n.666+76056_666+76058delinsGTT
XM_017001261.2:c.666+76056_666+76058delinsGTT	XP_016856750.1:n.666+76056_666+76058delinsGTT
XM_017001262.2:c.666+76056_666+76058delinsGTT	XP_016856751.1:n.666+76056_666+76058delinsGTT
XM_024446933.1:c.666+76056_666+76058delinsGTT	XP_024302701.1:n.666+76056_666+76058delinsGTT
XM_024446935.1:c.666+76056_666+76058delinsGTT	XP_024302703.1:n.666+76056_666+76058delinsGTT
XR_946654.3:n.1244+76056_1244+76058delinsGTT
NM_001194986.2:c.666+76056_666+76058delinsGTT MANE Select	NP_001181915.1:n.666+76056_666+76058delinsGTT