Canonical Allele Identifier: CA358450628

Gene: LRBA

Linked Data

• MyVariant Identifiers: chr4:g.151765319C>G (hg19) ; chr4:g.150844167C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.150844167C>G , CM000666.2:g.150844167C>G	GRCh38
NC_000004.11:g.151765319C>G , CM000666.1:g.151765319C>G	GRCh37
NC_000004.10:g.151984769C>G	NCBI36
NG_032855.1:g.176331G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651695.2:c.4502G>C	ENSP00000498254.2:p.Arg1501Thr
ENST00000697129.1:n.2829G>C
ENST00000357115.9:c.4502G>C	ENSP00000349629.3:p.Arg1501Thr
ENST00000651035.1:c.4502G>C	ENSP00000498673.1:p.Arg1501Thr
ENST00000651695.1:c.2216G>C	ENSP00000498254.1:p.Arg739Thr
ENST00000651943.2:c.4502G>C MANE Select	ENSP00000498582.2:p.Arg1501Thr
ENST00000357115.7:c.4502G>C	ENSP00000349629.3:p.Arg1501Thr
ENST00000502839.1:c.233G>C	ENSP00000424640.1:p.Arg78Thr
ENST00000507224.5:c.4502G>C	ENSP00000422180.1:p.Arg1501Thr
ENST00000509835.5:c.460G>C
ENST00000510413.5:c.4502G>C	ENSP00000421552.1:p.Arg1501Thr
NM_001199282.2:c.4502G>C	NP_001186211.2:p.Arg1501Thr
NM_006726.4:c.4502G>C	NP_006717.2:p.Arg1501Thr
XM_005263372.2:c.4502G>C	XP_005263429.1:p.Arg1501Thr
XM_005263373.1:c.4502G>C	XP_005263430.1:p.Arg1501Thr
XM_005263374.2:c.4502G>C	XP_005263431.1:p.Arg1501Thr
XM_005263375.2:c.4502G>C	XP_005263432.1:p.Arg1501Thr
XM_005263377.2:c.4502G>C	XP_005263434.1:p.Arg1501Thr
XM_011532434.1:c.4502G>C	XP_011530736.1:p.Arg1501Thr
NM_001364905.1:c.4502G>C MANE Select	NP_001351834.1:p.Arg1501Thr
XM_005263372.3:c.4502G>C	XP_005263429.1:p.Arg1501Thr
XM_005263373.3:c.4502G>C	XP_005263430.1:p.Arg1501Thr
XM_005263374.3:c.4502G>C	XP_005263431.1:p.Arg1501Thr
XM_011532434.2:c.4502G>C	XP_011530736.1:p.Arg1501Thr
XM_017008872.2:c.4502G>C	XP_016864361.1:p.Arg1501Thr
NM_001367550.1:c.4502G>C	NP_001354479.1:p.Arg1501Thr