Canonical Allele Identifier: CA2684801191

Gene: GARIN1B

Linked Data

• gnomAD v4: 7-128723063-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723063T>A , CM000669.2:g.128723063T>A	GRCh38
NC_000007.13:g.128363117T>A , CM000669.1:g.128363117T>A	GRCh37
NC_000007.12:g.128150353T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621392.5:c.688-134T>A MANE Select	ENSP00000477573.2:n.688-134T>A
ENST00000315184.9:c.688-134T>A	ENSP00000326652.4:n.688-134T>A
ENST00000466842.1:c.256-134T>A	ENSP00000417930.1:n.256-134T>A
ENST00000469348.5:n.547-134T>A
ENST00000471558.5:c.688-134T>A	ENSP00000418672.1:n.688-134T>A
ENST00000484425.6:c.259-134T>A	ENSP00000418591.2:n.259-134T>A
ENST00000485070.5:c.391-134T>A	ENSP00000418192.1:n.391-134T>A
ENST00000493738.5:n.644-134T>A
ENST00000621392.4:c.391-134T>A	ENSP00000477573.1:n.391-134T>A
NM_001282788.1:c.688-134T>A	NP_001269717.1:n.688-134T>A
NM_001282789.1:c.391-134T>A	NP_001269718.1:n.391-134T>A
NM_032599.3:c.688-134T>A	NP_115988.1:n.688-134T>A
NR_104242.1:n.788-134T>A
NR_104243.1:n.677-134T>A
XM_017012743.2:c.688-134T>A	XP_016868232.1:n.688-134T>A
XR_002956499.1:n.739-134T>A
NM_001282788.2:c.688-134T>A	NP_001269717.1:n.688-134T>A
NM_001282789.2:c.391-134T>A	NP_001269718.1:n.391-134T>A
NM_032599.4:c.688-134T>A	NP_115988.1:n.688-134T>A
NR_104242.2:n.739-134T>A
NR_104243.2:n.677-134T>A
NM_001282788.3:c.688-134T>A MANE Select	NP_001269717.1:n.688-134T>A