Canonical Allele Identifier: CA369196871

Gene: GARIN1B

Linked Data

• MyVariant Identifiers: chr7:g.128363329C>G (hg19) ; chr7:g.128723275C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723275C>G , CM000669.2:g.128723275C>G	GRCh38
NC_000007.13:g.128363329C>G , CM000669.1:g.128363329C>G	GRCh37
NC_000007.12:g.128150565C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621392.5:c.766C>G MANE Select	ENSP00000477573.2:p.Leu256Val
ENST00000315184.9:c.766C>G	ENSP00000326652.4:p.Leu256Val
ENST00000466842.1:c.334C>G	ENSP00000417930.1:p.Leu112Val
ENST00000469348.5:n.625C>G
ENST00000471558.5:c.766C>G	ENSP00000418672.1:p.Leu256Val
ENST00000484425.6:c.337C>G	ENSP00000418591.2:p.Leu113Val
ENST00000485070.5:c.469C>G	ENSP00000418192.1:p.Leu157Val
ENST00000493738.5:n.722C>G
ENST00000621392.4:c.469C>G	ENSP00000477573.1:p.Leu157Val
NM_001282788.1:c.766C>G	NP_001269717.1:p.Leu256Val
NM_001282789.1:c.469C>G	NP_001269718.1:p.Leu157Val
NM_032599.3:c.766C>G	NP_115988.1:p.Leu256Val
NR_104242.1:n.866C>G
NR_104243.1:n.755C>G
XM_017012743.2:c.766C>G	XP_016868232.1:p.Leu256Val
XR_002956499.1:n.817C>G
NM_001282788.2:c.766C>G	NP_001269717.1:p.Leu256Val
NM_001282789.2:c.469C>G	NP_001269718.1:p.Leu157Val
NM_032599.4:c.766C>G	NP_115988.1:p.Leu256Val
NR_104242.2:n.817C>G
NR_104243.2:n.755C>G
NM_001282788.3:c.766C>G MANE Select	NP_001269717.1:p.Leu256Val