Canonical Allele Identifier: CA441758318

Gene: LRBA

Linked Data

• gnomAD v4: 4-150844172-T-C
• MyVariant Identifiers: chr4:g.151765324T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.150844172T>C , CM000666.2:g.150844172T>C	GRCh38
NC_000004.11:g.151765324T>C , CM000666.1:g.151765324T>C	GRCh37
NC_000004.10:g.151984774T>C	NCBI36
NG_032855.1:g.176326A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651695.2:c.4497A>G	ENSP00000498254.2:p.Pro1499=
ENST00000697129.1:n.2824A>G
ENST00000357115.9:c.4497A>G	ENSP00000349629.3:p.Pro1499=
ENST00000651035.1:c.4497A>G	ENSP00000498673.1:p.Pro1499=
ENST00000651695.1:c.2211A>G	ENSP00000498254.1:p.Pro737=
ENST00000651943.2:c.4497A>G MANE Select	ENSP00000498582.2:p.Pro1499=
ENST00000357115.7:c.4497A>G	ENSP00000349629.3:p.Pro1499=
ENST00000502839.1:c.228A>G	ENSP00000424640.1:p.Pro76=
ENST00000507224.5:c.4497A>G	ENSP00000422180.1:p.Pro1499=
ENST00000509835.5:c.455A>G
ENST00000510413.5:c.4497A>G	ENSP00000421552.1:p.Pro1499=
NM_001199282.2:c.4497A>G	NP_001186211.2:p.Pro1499=
NM_006726.4:c.4497A>G	NP_006717.2:p.Pro1499=
XM_005263372.2:c.4497A>G	XP_005263429.1:p.Pro1499=
XM_005263373.1:c.4497A>G	XP_005263430.1:p.Pro1499=
XM_005263374.2:c.4497A>G	XP_005263431.1:p.Pro1499=
XM_005263375.2:c.4497A>G	XP_005263432.1:p.Pro1499=
XM_005263377.2:c.4497A>G	XP_005263434.1:p.Pro1499=
XM_011532434.1:c.4497A>G	XP_011530736.1:p.Pro1499=
NM_001364905.1:c.4497A>G MANE Select	NP_001351834.1:p.Pro1499=
XM_005263372.3:c.4497A>G	XP_005263429.1:p.Pro1499=
XM_005263373.3:c.4497A>G	XP_005263430.1:p.Pro1499=
XM_005263374.3:c.4497A>G	XP_005263431.1:p.Pro1499=
XM_011532434.2:c.4497A>G	XP_011530736.1:p.Pro1499=
XM_017008872.2:c.4497A>G	XP_016864361.1:p.Pro1499=
NM_001367550.1:c.4497A>G	NP_001354479.1:p.Pro1499=