Canonical Allele Identifier: CA369196773

Gene: GARIN1B

Linked Data

• MyVariant Identifiers: chr7:g.128363309C>A (hg19) ; chr7:g.128723255C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723255C>A , CM000669.2:g.128723255C>A	GRCh38
NC_000007.13:g.128363309C>A , CM000669.1:g.128363309C>A	GRCh37
NC_000007.12:g.128150545C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000621392.5:c.746C>A MANE Select	ENSP00000477573.2:p.Thr249Asn
ENST00000315184.9:c.746C>A	ENSP00000326652.4:p.Thr249Asn
ENST00000466842.1:c.314C>A	ENSP00000417930.1:p.Thr105Asn
ENST00000469348.5:n.605C>A
ENST00000471558.5:c.746C>A	ENSP00000418672.1:p.Thr249Asn
ENST00000484425.6:c.317C>A	ENSP00000418591.2:p.Thr106Asn
ENST00000485070.5:c.449C>A	ENSP00000418192.1:p.Thr150Asn
ENST00000493738.5:n.702C>A
ENST00000621392.4:c.449C>A	ENSP00000477573.1:p.Thr150Asn
NM_001282788.1:c.746C>A	NP_001269717.1:p.Thr249Asn
NM_001282789.1:c.449C>A	NP_001269718.1:p.Thr150Asn
NM_032599.3:c.746C>A	NP_115988.1:p.Thr249Asn
NR_104242.1:n.846C>A
NR_104243.1:n.735C>A
XM_017012743.2:c.746C>A	XP_016868232.1:p.Thr249Asn
XR_002956499.1:n.797C>A
NM_001282788.2:c.746C>A	NP_001269717.1:p.Thr249Asn
NM_001282789.2:c.449C>A	NP_001269718.1:p.Thr150Asn
NM_032599.4:c.746C>A	NP_115988.1:p.Thr249Asn
NR_104242.2:n.797C>A
NR_104243.2:n.735C>A
NM_001282788.3:c.746C>A MANE Select	NP_001269717.1:p.Thr249Asn