Canonical Allele Identifier: CA1742494458

Gene: GARIN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723106_128723110delinsTCCAA , CM000669.2:g.128723106_128723110delinsTCCAA	GRCh38
NC_000007.13:g.128363160_128363164delinsTCCAA , CM000669.1:g.128363160_128363164delinsTCCAA	GRCh37
NC_000007.12:g.128150396_128150400delinsTCCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621392.5:c.688-91_688-87delinsTCCAA MANE Select	ENSP00000477573.2:n.688-91_688-87delinsTCCAA
ENST00000315184.9:c.688-91_688-87delinsTCCAA	ENSP00000326652.4:n.688-91_688-87delinsTCCAA
ENST00000466842.1:c.256-91_256-87delinsTCCAA	ENSP00000417930.1:n.256-91_256-87delinsTCCAA
ENST00000469348.5:n.547-91_547-87delinsTCCAA
ENST00000471558.5:c.688-91_688-87delinsTCCAA	ENSP00000418672.1:n.688-91_688-87delinsTCCAA
ENST00000484425.6:c.259-91_259-87delinsTCCAA	ENSP00000418591.2:n.259-91_259-87delinsTCCAA
ENST00000485070.5:c.391-91_391-87delinsTCCAA	ENSP00000418192.1:n.391-91_391-87delinsTCCAA
ENST00000493738.5:n.644-91_644-87delinsTCCAA
ENST00000621392.4:c.391-91_391-87delinsTCCAA	ENSP00000477573.1:n.391-91_391-87delinsTCCAA
NM_001282788.1:c.688-91_688-87delinsTCCAA	NP_001269717.1:n.688-91_688-87delinsTCCAA
NM_001282789.1:c.391-91_391-87delinsTCCAA	NP_001269718.1:n.391-91_391-87delinsTCCAA
NM_032599.3:c.688-91_688-87delinsTCCAA	NP_115988.1:n.688-91_688-87delinsTCCAA
NR_104242.1:n.788-91_788-87delinsTCCAA
NR_104243.1:n.677-91_677-87delinsTCCAA
XM_017012743.2:c.688-91_688-87delinsTCCAA	XP_016868232.1:n.688-91_688-87delinsTCCAA
XR_002956499.1:n.739-91_739-87delinsTCCAA
NM_001282788.2:c.688-91_688-87delinsTCCAA	NP_001269717.1:n.688-91_688-87delinsTCCAA
NM_001282789.2:c.391-91_391-87delinsTCCAA	NP_001269718.1:n.391-91_391-87delinsTCCAA
NM_032599.4:c.688-91_688-87delinsTCCAA	NP_115988.1:n.688-91_688-87delinsTCCAA
NR_104242.2:n.739-91_739-87delinsTCCAA
NR_104243.2:n.677-91_677-87delinsTCCAA
NM_001282788.3:c.688-91_688-87delinsTCCAA MANE Select	NP_001269717.1:n.688-91_688-87delinsTCCAA