Canonical Allele Identifier: CA457551122

Gene: GARIN1B

Linked Data

• MyVariant Identifiers: chr7:g.128363302C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723248C>T , CM000669.2:g.128723248C>T	GRCh38
NC_000007.13:g.128363302C>T , CM000669.1:g.128363302C>T	GRCh37
NC_000007.12:g.128150538C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000621392.5:c.739C>T MANE Select	ENSP00000477573.2:p.Leu247=
ENST00000315184.9:c.739C>T	ENSP00000326652.4:p.Leu247=
ENST00000466842.1:c.307C>T	ENSP00000417930.1:p.Leu103=
ENST00000469348.5:n.598C>T
ENST00000471558.5:c.739C>T	ENSP00000418672.1:p.Leu247=
ENST00000484425.6:c.310C>T	ENSP00000418591.2:p.Leu104=
ENST00000485070.5:c.442C>T	ENSP00000418192.1:p.Leu148=
ENST00000493738.5:n.695C>T
ENST00000621392.4:c.442C>T	ENSP00000477573.1:p.Leu148=
NM_001282788.1:c.739C>T	NP_001269717.1:p.Leu247=
NM_001282789.1:c.442C>T	NP_001269718.1:p.Leu148=
NM_032599.3:c.739C>T	NP_115988.1:p.Leu247=
NR_104242.1:n.839C>T
NR_104243.1:n.728C>T
XM_017012743.2:c.739C>T	XP_016868232.1:p.Leu247=
XR_002956499.1:n.790C>T
NM_001282788.2:c.739C>T	NP_001269717.1:p.Leu247=
NM_001282789.2:c.442C>T	NP_001269718.1:p.Leu148=
NM_032599.4:c.739C>T	NP_115988.1:p.Leu247=
NR_104242.2:n.790C>T
NR_104243.2:n.728C>T
NM_001282788.3:c.739C>T MANE Select	NP_001269717.1:p.Leu247=