Canonical Allele Identifier: CA1742494438

Gene: GARIN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723061_128723063delinsCCT , CM000669.2:g.128723061_128723063delinsCCT	GRCh38
NC_000007.13:g.128363115_128363117delinsCCT , CM000669.1:g.128363115_128363117delinsCCT	GRCh37
NC_000007.12:g.128150351_128150353delinsCCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621392.5:c.688-136_688-134delinsCCT MANE Select	ENSP00000477573.2:n.688-136_688-134delinsCCT
ENST00000315184.9:c.688-136_688-134delinsCCT	ENSP00000326652.4:n.688-136_688-134delinsCCT
ENST00000466842.1:c.256-136_256-134delinsCCT	ENSP00000417930.1:n.256-136_256-134delinsCCT
ENST00000469348.5:n.547-136_547-134delinsCCT
ENST00000471558.5:c.688-136_688-134delinsCCT	ENSP00000418672.1:n.688-136_688-134delinsCCT
ENST00000484425.6:c.259-136_259-134delinsCCT	ENSP00000418591.2:n.259-136_259-134delinsCCT
ENST00000485070.5:c.391-136_391-134delinsCCT	ENSP00000418192.1:n.391-136_391-134delinsCCT
ENST00000493738.5:n.644-136_644-134delinsCCT
ENST00000621392.4:c.391-136_391-134delinsCCT	ENSP00000477573.1:n.391-136_391-134delinsCCT
NM_001282788.1:c.688-136_688-134delinsCCT	NP_001269717.1:n.688-136_688-134delinsCCT
NM_001282789.1:c.391-136_391-134delinsCCT	NP_001269718.1:n.391-136_391-134delinsCCT
NM_032599.3:c.688-136_688-134delinsCCT	NP_115988.1:n.688-136_688-134delinsCCT
NR_104242.1:n.788-136_788-134delinsCCT
NR_104243.1:n.677-136_677-134delinsCCT
XM_017012743.2:c.688-136_688-134delinsCCT	XP_016868232.1:n.688-136_688-134delinsCCT
XR_002956499.1:n.739-136_739-134delinsCCT
NM_001282788.2:c.688-136_688-134delinsCCT	NP_001269717.1:n.688-136_688-134delinsCCT
NM_001282789.2:c.391-136_391-134delinsCCT	NP_001269718.1:n.391-136_391-134delinsCCT
NM_032599.4:c.688-136_688-134delinsCCT	NP_115988.1:n.688-136_688-134delinsCCT
NR_104242.2:n.739-136_739-134delinsCCT
NR_104243.2:n.677-136_677-134delinsCCT
NM_001282788.3:c.688-136_688-134delinsCCT MANE Select	NP_001269717.1:n.688-136_688-134delinsCCT