Canonical Allele Identifier: CA1503629015

Gene: LRBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.150844445_150844446delinsCA , CM000666.2:g.150844445_150844446delinsCA	GRCh38
NC_000004.11:g.151765597_151765598delinsCA , CM000666.1:g.151765597_151765598delinsCA	GRCh37
NC_000004.10:g.151985047_151985048delinsCA	NCBI36
NG_032855.1:g.176052_176053delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651695.2:c.4461+212_4461+213delinsTG	ENSP00000498254.2:n.4461+212_4461+213delinsTG
ENST00000697129.1:n.2788+212_2788+213delinsTG
ENST00000357115.9:c.4461+212_4461+213delinsTG	ENSP00000349629.3:n.4461+212_4461+213delinsTG
ENST00000651035.1:c.4461+212_4461+213delinsTG	ENSP00000498673.1:n.4461+212_4461+213delinsTG
ENST00000651695.1:c.2175+212_2175+213delinsTG	ENSP00000498254.1:n.2175+212_2175+213delinsTG
ENST00000651943.2:c.4461+212_4461+213delinsTG MANE Select	ENSP00000498582.2:n.4461+212_4461+213delinsTG
ENST00000357115.7:c.4461+212_4461+213delinsTG	ENSP00000349629.3:n.4461+212_4461+213delinsTG
ENST00000502839.1:c.192+212_192+213delinsTG	ENSP00000424640.1:n.192+212_192+213delinsTG
ENST00000507224.5:c.4461+212_4461+213delinsTG	ENSP00000422180.1:n.4461+212_4461+213delinsTG
ENST00000509835.5:c.419+212_419+213delinsTG
ENST00000510413.5:c.4461+212_4461+213delinsTG	ENSP00000421552.1:n.4461+212_4461+213delinsTG
NM_001199282.2:c.4461+212_4461+213delinsTG	NP_001186211.2:n.4461+212_4461+213delinsTG
NM_006726.4:c.4461+212_4461+213delinsTG	NP_006717.2:n.4461+212_4461+213delinsTG
XM_005263372.2:c.4461+212_4461+213delinsTG	XP_005263429.1:n.4461+212_4461+213delinsTG
XM_005263373.1:c.4461+212_4461+213delinsTG	XP_005263430.1:n.4461+212_4461+213delinsTG
XM_005263374.2:c.4461+212_4461+213delinsTG	XP_005263431.1:n.4461+212_4461+213delinsTG
XM_005263375.2:c.4461+212_4461+213delinsTG	XP_005263432.1:n.4461+212_4461+213delinsTG
XM_005263377.2:c.4461+212_4461+213delinsTG	XP_005263434.1:n.4461+212_4461+213delinsTG
XM_011532434.1:c.4461+212_4461+213delinsTG	XP_011530736.1:n.4461+212_4461+213delinsTG
NM_001364905.1:c.4461+212_4461+213delinsTG MANE Select	NP_001351834.1:n.4461+212_4461+213delinsTG
XM_005263372.3:c.4461+212_4461+213delinsTG	XP_005263429.1:n.4461+212_4461+213delinsTG
XM_005263373.3:c.4461+212_4461+213delinsTG	XP_005263430.1:n.4461+212_4461+213delinsTG
XM_005263374.3:c.4461+212_4461+213delinsTG	XP_005263431.1:n.4461+212_4461+213delinsTG
XM_011532434.2:c.4461+212_4461+213delinsTG	XP_011530736.1:n.4461+212_4461+213delinsTG
XM_017008872.2:c.4461+212_4461+213delinsTG	XP_016864361.1:n.4461+212_4461+213delinsTG
NM_001367550.1:c.4461+212_4461+213delinsTG	NP_001354479.1:n.4461+212_4461+213delinsTG