Canonical Allele Identifier: CA453455072

Gene: BRAT1

Linked Data

• gnomAD v4: 7-2539856-C-T
• MyVariant Identifiers: chr7:g.2579490C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2539856C>T , CM000669.2:g.2539856C>T	GRCh38
NC_000007.13:g.2579490C>T , CM000669.1:g.2579490C>T	GRCh37
NC_000007.12:g.2546016C>T	NCBI36
NG_032167.1:g.20903G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340611.9:c.1428G>A MANE Select	ENSP00000339637.4:p.Arg476=
ENST00000340611.8:c.1428G>A	ENSP00000339637.4:p.Arg476=
ENST00000467558.5:n.2800G>A
ENST00000469750.5:n.4000G>A
ENST00000473879.1:n.144G>A
ENST00000493232.5:n.4164G>A
NM_152743.3:c.1428G>A	NP_689956.2:p.Arg476=
XM_005249643.3:c.1428G>A	XP_005249700.1:p.Arg476=
XM_011515177.1:c.1512G>A	XP_011513479.1:p.Arg504=
XM_011515178.1:c.1512G>A	XP_011513480.1:p.Arg504=
XM_011515179.1:c.1509G>A	XP_011513481.1:p.Arg503=
XM_011515180.1:c.1482G>A	XP_011513482.1:p.Arg494=
XM_011515181.1:c.1512G>A	XP_011513483.1:p.Arg504=
XM_011515182.1:c.1512G>A	XP_011513484.1:p.Arg504=
XM_011515183.1:c.987G>A	XP_011513485.1:p.Arg329=
XM_011515184.1:c.987G>A	XP_011513486.1:p.Arg329=
XM_011515185.1:c.1428G>A	XP_011513487.1:p.Arg476=
XM_011515186.1:c.1512G>A	XP_011513488.1:p.Arg504=
XM_011515187.1:c.84G>A	XP_011513489.1:p.Arg28=
NM_001350626.1:c.1428G>A	NP_001337555.1:p.Arg476=
NM_001350627.1:c.903G>A	NP_001337556.1:p.Arg301=
NR_146879.1:n.1845G>A
XM_011515177.2:c.1512G>A	XP_011513479.1:p.Arg504=
XM_011515179.2:c.1509G>A	XP_011513481.1:p.Arg503=
XM_011515181.2:c.1512G>A	XP_011513483.1:p.Arg504=
XM_011515182.2:c.1512G>A	XP_011513484.1:p.Arg504=
XM_011515184.3:c.987G>A	XP_011513486.1:p.Arg329=
XM_011515186.2:c.1512G>A	XP_011513488.1:p.Arg504=
XM_017011833.1:c.1425G>A	XP_016867322.1:p.Arg475=
XM_017011834.1:c.1425G>A	XP_016867323.1:p.Arg475=
XM_017011836.2:c.1428G>A	XP_016867325.1:p.Arg476=
XM_024446682.1:c.84G>A	XP_024302450.1:p.Arg28=
NM_152743.4:c.1428G>A MANE Select	NP_689956.2:p.Arg476=
NM_001350626.2:c.1428G>A	NP_001337555.1:p.Arg476=
NM_001350627.2:c.903G>A	NP_001337556.1:p.Arg301=
NR_146879.2:n.1611G>A