Canonical Allele Identifier: CA1540444240

Gene: OSMR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38923237G= , CM000667.2:g.38923237G=	GRCh38
NC_000005.9:g.38923339G= , CM000667.1:g.38923339G=	GRCh37
NC_000005.8:g.38959096G=	NCBI36
NG_016236.1:g.82380G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274276.8:c.1853G= MANE Select	ENSP00000274276.3:p.Gly618=
ENST00000274276.7:c.1853G=	ENSP00000274276.3:p.Gly618=
NM_003999.2:c.1853G=	NP_003990.1:p.Gly618=
XM_005248384.1:c.1856G=	XP_005248441.1:p.Gly619=
XM_005248385.1:c.1856G=	XP_005248442.1:p.Gly619=
XM_011514161.1:c.1856G=	XP_011512463.1:p.Gly619=
XR_925661.1:n.2245G=
NM_001323505.1:c.1853G=	NP_001310434.1:p.Gly618=
NM_001323506.1:c.1856G=	NP_001310435.1:p.Gly619=
XM_011514161.2:c.1856G=	XP_011512463.1:p.Gly619=
XM_017010019.1:c.1853G=	XP_016865508.1:p.Gly618=
NM_003999.3:c.1853G= MANE Select	NP_003990.1:p.Gly618=
NM_001323505.2:c.1853G=	NP_001310434.1:p.Gly618=
NM_001323506.2:c.1856G=	NP_001310435.1:p.Gly619=