Canonical Allele Identifier: CA10496418

Gene: LRCH2 RBMXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.115191663A>G , CM000685.2:g.115191663A>G	GRCh38
NC_000023.10:g.114426226A>G , CM000685.1:g.114426226A>G	GRCh37
NC_000023.9:g.114332482A>G	NCBI36
NG_021299.1:g.47410T>C
NG_021299.2:g.47410T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001145346.2:c.2222A>G (RBMXL3) MANE Select	NP_001138818.1:p.Tyr741Cys
NM_020871.4:c.350-3293T>C (LRCH2) MANE Select	NP_065922.3:n.350-3293T>C
ENST00000317135.13:c.350-3293T>C (LRCH2) MANE Select	ENSP00000325091.8:n.350-3293T>C
ENST00000424776.5:c.2222A>G (RBMXL3) MANE Select	ENSP00000417451.3:p.Tyr741Cys
NM_001145346.1:c.2222A>G (RBMXL3)	NP_001138818.1:p.Tyr741Cys
NM_001243963.1:c.350-3293T>C (LRCH2)	NP_001230892.1:n.350-3293T>C
NM_001243963.2:c.350-3293T>C (LRCH2)	NP_001230892.1:n.350-3293T>C
NM_020871.3:c.350-3293T>C (LRCH2)	NP_065922.3:n.350-3293T>C
ENST00000317135.12:c.350-3293T>C (LRCH2)	ENSP00000325091.8:n.350-3293T>C
ENST00000424776.4:c.2222A>G (RBMXL3)	ENSP00000417451.2:p.Tyr741Cys
ENST00000538422.2:c.350-3293T>C (LRCH2)	ENSP00000439366.1:n.350-3293T>C
XM_006724724.2:c.350-3293T>C (LRCH2)	XP_006724787.2:n.350-3293T>C
XM_006724724.3:c.350-3293T>C (LRCH2)	XP_006724787.2:n.350-3293T>C
XM_017029696.2:c.350-3293T>C (LRCH2)	XP_016885185.1:n.350-3293T>C