Canonical Allele Identifier: CA1742494483

Gene: GARIN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723159_128723160delinsGC , CM000669.2:g.128723159_128723160delinsGC	GRCh38
NC_000007.13:g.128363213_128363214delinsGC , CM000669.1:g.128363213_128363214delinsGC	GRCh37
NC_000007.12:g.128150449_128150450delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000621392.5:c.688-38_688-37delinsGC MANE Select	ENSP00000477573.2:n.688-38_688-37delinsGC...
ENST00000315184.9:c.688-38_688-37delinsGC	ENSP00000326652.4:n.688-38_688-37delinsGC...
ENST00000466842.1:c.256-38_256-37delinsGC	ENSP00000417930.1:n.256-38_256-37delinsGC...
ENST00000469348.5:n.547-38_547-37delinsGC
ENST00000471558.5:c.688-38_688-37delinsGC	ENSP00000418672.1:n.688-38_688-37delinsGC...
ENST00000484425.6:c.259-38_259-37delinsGC	ENSP00000418591.2:n.259-38_259-37delinsGC...
ENST00000485070.5:c.391-38_391-37delinsGC	ENSP00000418192.1:n.391-38_391-37delinsGC...
ENST00000493738.5:n.644-38_644-37delinsGC
ENST00000621392.4:c.391-38_391-37delinsGC	ENSP00000477573.1:n.391-38_391-37delinsGC...
NM_001282788.1:c.688-38_688-37delinsGC	NP_001269717.1:n.688-38_688-37delinsGC
NM_001282789.1:c.391-38_391-37delinsGC	NP_001269718.1:n.391-38_391-37delinsGC
NM_032599.3:c.688-38_688-37delinsGC	NP_115988.1:n.688-38_688-37delinsGC
NR_104242.1:n.788-38_788-37delinsGC
NR_104243.1:n.677-38_677-37delinsGC
XM_017012743.2:c.688-38_688-37delinsGC	XP_016868232.1:n.688-38_688-37delinsGC
XR_002956499.1:n.739-38_739-37delinsGC
NM_001282788.2:c.688-38_688-37delinsGC	NP_001269717.1:n.688-38_688-37delinsGC
NM_001282789.2:c.391-38_391-37delinsGC	NP_001269718.1:n.391-38_391-37delinsGC
NM_032599.4:c.688-38_688-37delinsGC	NP_115988.1:n.688-38_688-37delinsGC
NR_104242.2:n.739-38_739-37delinsGC
NR_104243.2:n.677-38_677-37delinsGC
NM_001282788.3:c.688-38_688-37delinsGC MANE Select	NP_001269717.1:n.688-38_688-37delinsGC