Canonical Allele Identifier: CA2257383487

Gene: UNC45B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35151166C= , CM000679.2:g.35151166C=	GRCh38
NC_000017.10:g.33478185C= , CM000679.1:g.33478185C=	GRCh37
NC_000017.9:g.30502298C=	NCBI36
NG_042129.1:g.8350C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001267052.2:c.381+943C= MANE Select	NP_001253981.1:n.381+943C=
ENST00000394570.7:c.381+943C= MANE Select	ENSP00000378071.2:n.381+943C=
NM_001033576.1:c.381+943C=	NP_001028748.1:n.381+943C=
NM_001033576.2:c.381+943C=	NP_001028748.1:n.381+943C=
NM_001267052.1:c.381+943C=	NP_001253981.1:n.381+943C=
NM_001308281.1:c.381+943C=	NP_001295210.1:n.381+943C=
NM_173167.2:c.381+943C=	NP_775259.1:n.381+943C=
NM_173167.3:c.381+943C=	NP_775259.1:n.381+943C=
ENST00000268876.9:c.381+943C=	ENSP00000268876.4:n.381+943C=
ENST00000394570.6:c.381+943C=	ENSP00000378071.2:n.381+943C=
ENST00000591048.2:c.381+943C=	ENSP00000468335.1:n.381+943C=
XM_017024234.1:c.381+943C=	XP_016879723.1:n.381+943C=