Canonical Allele Identifier: CA1742494439

Gene: GARIN1B

Linked Data

• dbSNP Id: rs1799606511

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723064_128723065del , CM000669.2:g.128723064_128723065del	GRCh38
NC_000007.13:g.128363118_128363119del , CM000669.1:g.128363118_128363119del	GRCh37
NC_000007.12:g.128150354_128150355del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000621392.5:c.688-133_688-132del MANE Select	ENSP00000477573.2:n.688-133_688-132del
ENST00000315184.9:c.688-133_688-132del	ENSP00000326652.4:n.688-133_688-132del
ENST00000466842.1:c.256-133_256-132del	ENSP00000417930.1:n.256-133_256-132del
ENST00000469348.5:n.547-133_547-132del
ENST00000471558.5:c.688-133_688-132del	ENSP00000418672.1:n.688-133_688-132del
ENST00000484425.6:c.259-133_259-132del	ENSP00000418591.2:n.259-133_259-132del
ENST00000485070.5:c.391-133_391-132del	ENSP00000418192.1:n.391-133_391-132del
ENST00000493738.5:n.644-133_644-132del
ENST00000621392.4:c.391-133_391-132del	ENSP00000477573.1:n.391-133_391-132del
NM_001282788.1:c.688-133_688-132del	NP_001269717.1:n.688-133_688-132del
NM_001282789.1:c.391-133_391-132del	NP_001269718.1:n.391-133_391-132del
NM_032599.3:c.688-133_688-132del	NP_115988.1:n.688-133_688-132del
NR_104242.1:n.788-133_788-132del
NR_104243.1:n.677-133_677-132del
XM_017012743.2:c.688-133_688-132del	XP_016868232.1:n.688-133_688-132del
XR_002956499.1:n.739-133_739-132del
NM_001282788.2:c.688-133_688-132del	NP_001269717.1:n.688-133_688-132del
NM_001282789.2:c.391-133_391-132del	NP_001269718.1:n.391-133_391-132del
NM_032599.4:c.688-133_688-132del	NP_115988.1:n.688-133_688-132del
NR_104242.2:n.739-133_739-132del
NR_104243.2:n.677-133_677-132del
NM_001282788.3:c.688-133_688-132del MANE Select	NP_001269717.1:n.688-133_688-132del