Canonical Allele Identifier: CA1165879768

Gene: AGBL4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.49977732_49977734delinsTCA , CM000663.2:g.49977732_49977734delinsTCA	GRCh38
NC_000001.10:g.50443404_50443406delinsTCA , CM000663.1:g.50443404_50443406delinsTCA	GRCh37
NC_000001.9:g.50215991_50215993delinsTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371839.6:c.34+46029_34+46031delinsTGA MANE Select	ENSP00000360905.1:n.34+46029_34+46031delinsTGA
ENST00000371836.1:c.34+46029_34+46031delinsTGA	ENSP00000360902.1:n.34+46029_34+46031delinsTGA
ENST00000371838.5:c.34+46029_34+46031delinsTGA	ENSP00000360904.1:n.34+46029_34+46031delinsTGA
ENST00000371839.5:c.34+46029_34+46031delinsTGA	ENSP00000360905.1:n.34+46029_34+46031delinsTGA
NM_032785.3:c.34+46029_34+46031delinsTGA	NP_116174.3:n.34+46029_34+46031delinsTGA
XM_006710986.2:c.34+46029_34+46031delinsTGA	XP_006711049.1:n.34+46029_34+46031delinsTGA
XM_011542308.1:c.34+46029_34+46031delinsTGA	XP_011540610.1:n.34+46029_34+46031delinsTGA
XM_011542309.1:c.34+46029_34+46031delinsTGA	XP_011540611.1:n.34+46029_34+46031delinsTGA
XM_011542310.1:c.34+46029_34+46031delinsTGA	XP_011540612.1:n.34+46029_34+46031delinsTGA
XM_011542311.1:c.34+46029_34+46031delinsTGA	XP_011540613.1:n.34+46029_34+46031delinsTGA
NM_001323573.1:c.34+46029_34+46031delinsTGA	NP_001310502.1:n.34+46029_34+46031delinsTGA
NM_001323574.1:c.34+46029_34+46031delinsTGA	NP_001310503.1:n.34+46029_34+46031delinsTGA
NM_001323575.1:c.34+46029_34+46031delinsTGA	NP_001310504.1:n.34+46029_34+46031delinsTGA
NR_136623.1:n.192+46029_192+46031delinsTGA
XM_011542308.2:c.34+46029_34+46031delinsTGA	XP_011540610.1:n.34+46029_34+46031delinsTGA
XM_011542310.2:c.34+46029_34+46031delinsTGA	XP_011540612.1:n.34+46029_34+46031delinsTGA
XM_017002595.2:c.34+46029_34+46031delinsTGA	XP_016858084.1:n.34+46029_34+46031delinsTGA
XM_017002596.2:c.34+46029_34+46031delinsTGA	XP_016858085.1:n.34+46029_34+46031delinsTGA
XM_017002597.2:c.34+46029_34+46031delinsTGA	XP_016858086.1:n.34+46029_34+46031delinsTGA
XM_017002598.2:c.34+46029_34+46031delinsTGA	XP_016858087.1:n.34+46029_34+46031delinsTGA
XM_024450399.1:c.34+46029_34+46031delinsTGA	XP_024306167.1:n.34+46029_34+46031delinsTGA
NM_032785.4:c.34+46029_34+46031delinsTGA MANE Select	NP_116174.3:n.34+46029_34+46031delinsTGA
NM_001323573.2:c.34+46029_34+46031delinsTGA	NP_001310502.1:n.34+46029_34+46031delinsTGA
NM_001323574.2:c.34+46029_34+46031delinsTGA	NP_001310503.1:n.34+46029_34+46031delinsTGA
NM_001323575.2:c.34+46029_34+46031delinsTGA	NP_001310504.1:n.34+46029_34+46031delinsTGA
NR_136623.2:n.192+46029_192+46031delinsTGA