Canonical Allele Identifier: CA1742494526

Gene: GARIN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723259G= , CM000669.2:g.128723259G=	GRCh38
NC_000007.13:g.128363313G= , CM000669.1:g.128363313G=	GRCh37
NC_000007.12:g.128150549G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621392.5:c.750G= MANE Select	ENSP00000477573.2:p.Lys250=
ENST00000315184.9:c.750G=	ENSP00000326652.4:p.Lys250=
ENST00000466842.1:c.318G=	ENSP00000417930.1:p.Lys106=
ENST00000469348.5:n.609G=
ENST00000471558.5:c.750G=	ENSP00000418672.1:p.Lys250=
ENST00000484425.6:c.321G=	ENSP00000418591.2:p.Lys107=
ENST00000485070.5:c.453G=	ENSP00000418192.1:p.Lys151=
ENST00000493738.5:n.706G=
ENST00000621392.4:c.453G=	ENSP00000477573.1:p.Lys151=
NM_001282788.1:c.750G=	NP_001269717.1:p.Lys250=
NM_001282789.1:c.453G=	NP_001269718.1:p.Lys151=
NM_032599.3:c.750G=	NP_115988.1:p.Lys250=
NR_104242.1:n.850G=
NR_104243.1:n.739G=
XM_017012743.2:c.750G=	XP_016868232.1:p.Lys250=
XR_002956499.1:n.801G=
NM_001282788.2:c.750G=	NP_001269717.1:p.Lys250=
NM_001282789.2:c.453G=	NP_001269718.1:p.Lys151=
NM_032599.4:c.750G=	NP_115988.1:p.Lys250=
NR_104242.2:n.801G=
NR_104243.2:n.739G=
NM_001282788.3:c.750G= MANE Select	NP_001269717.1:p.Lys250=