Canonical Allele Identifier: CA358436801

Gene: LRBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.150265782G>C , CM000666.2:g.150265782G>C	GRCh38
NC_000004.11:g.151186934G>C , CM000666.1:g.151186934G>C	GRCh37
NC_000004.10:g.151406384G>C	NCBI36
NG_032855.1:g.754716C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001364905.1:c.8499C>G MANE Select	NP_001351834.1:p.Ser2833Arg
ENST00000651943.2:c.8499C>G MANE Select	ENSP00000498582.2:p.Ser2833Arg
NM_001199282.2:c.8496C>G	NP_001186211.2:p.Ser2832Arg
NM_001367550.1:c.8514C>G	NP_001354479.1:p.Ser2838Arg
NM_006726.4:c.8532C>G	NP_006717.2:p.Ser2844Arg
ENST00000357115.7:c.8532C>G	ENSP00000349629.3:p.Ser2844Arg
ENST00000357115.9:c.8532C>G	ENSP00000349629.3:p.Ser2844Arg
ENST00000503716.5:n.2589C>G
ENST00000508606.1:c.417C>G
ENST00000509835.5:c.4457C>G
ENST00000510157.1:n.880C>G
ENST00000510157.2:n.1115C>G
ENST00000510413.5:c.8496C>G	ENSP00000421552.1:p.Ser2832Arg
ENST00000515096.5:n.1791C>G
ENST00000515096.6:n.5169C>G
ENST00000648626.1:n.2964C>G
ENST00000648823.1:c.2229C>G
ENST00000648878.1:c.2035C>G	ENSP00000497002.1:p.His679Asp
ENST00000651035.1:c.*2860C>G	ENSP00000498673.1:n.*2860C>G
ENST00000651695.1:c.6228C>G	ENSP00000498254.1:p.Ser2076Arg
ENST00000651695.2:c.8514C>G	ENSP00000498254.2:p.Ser2838Arg
ENST00000697127.1:c.2172C>G	ENSP00000513124.1:p.Ser724Arg
ENST00000697128.1:c.2848C>G
XM_005263372.2:c.8547C>G	XP_005263429.1:p.Ser2849Arg
XM_005263372.3:c.8547C>G	XP_005263429.1:p.Ser2849Arg
XM_005263373.1:c.8547C>G	XP_005263430.1:p.Ser2849Arg
XM_005263373.3:c.8547C>G	XP_005263430.1:p.Ser2849Arg
XM_005263374.2:c.8514C>G	XP_005263431.1:p.Ser2838Arg
XM_005263374.3:c.8514C>G	XP_005263431.1:p.Ser2838Arg
XM_005263375.2:c.8499C>G	XP_005263432.1:p.Ser2833Arg
XM_011532434.1:c.8532C>G	XP_011530736.1:p.Ser2844Arg
XM_011532434.2:c.8532C>G	XP_011530736.1:p.Ser2844Arg
XM_017008872.2:c.8514C>G	XP_016864361.1:p.Ser2838Arg
XM_017008873.2:c.2217C>G	XP_016864362.1:p.Ser739Arg
XM_017008874.1:c.2211C>G	XP_016864363.1:p.Ser737Arg