Canonical Allele Identifier: CA1742494496
Gene: GARIN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128723183T= , CM000669.2:g.128723183T= GRCh38
NC_000007.13:g.128363237T= , CM000669.1:g.128363237T= GRCh37
NC_000007.12:g.128150473T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000621392.5:c.688-14T= MANE Select ENSP00000477573.2:n.688-14T=
ENST00000315184.9:c.688-14T= ENSP00000326652.4:n.688-14T=
ENST00000466842.1:c.256-14T= ENSP00000417930.1:n.256-14T=
ENST00000469348.5:n.547-14T=
ENST00000471558.5:c.688-14T= ENSP00000418672.1:n.688-14T=
ENST00000484425.6:c.259-14T= ENSP00000418591.2:n.259-14T=
ENST00000485070.5:c.391-14T= ENSP00000418192.1:n.391-14T=
ENST00000493738.5:n.644-14T=
ENST00000621392.4:c.391-14T= ENSP00000477573.1:n.391-14T=
NM_001282788.1:c.688-14T= NP_001269717.1:n.688-14T=
NM_001282789.1:c.391-14T= NP_001269718.1:n.391-14T=
NM_032599.3:c.688-14T= NP_115988.1:n.688-14T=
NR_104242.1:n.788-14T=
NR_104243.1:n.677-14T=
XM_017012743.2:c.688-14T= XP_016868232.1:n.688-14T=
XR_002956499.1:n.739-14T=
NM_001282788.2:c.688-14T= NP_001269717.1:n.688-14T=
NM_001282789.2:c.391-14T= NP_001269718.1:n.391-14T=
NM_032599.4:c.688-14T= NP_115988.1:n.688-14T=
NR_104242.2:n.739-14T=
NR_104243.2:n.677-14T=
NM_001282788.3:c.688-14T= MANE Select NP_001269717.1:n.688-14T=