Canonical Allele Identifier: CA152666258

Gene: BRAT1

Linked Data

• dbSNP Id: rs374233073
• MyVariant Identifiers: chr7:g.2579472G>C (hg19) ; chr7:g.2539838G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2539838G>C , CM000669.2:g.2539838G>C	GRCh38
NC_000007.13:g.2579472G>C , CM000669.1:g.2579472G>C	GRCh37
NC_000007.12:g.2545998G>C	NCBI36
NG_032167.1:g.20921C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340611.9:c.1446C>G MANE Select	ENSP00000339637.4:p.Pro482=
ENST00000340611.8:c.1446C>G	ENSP00000339637.4:p.Pro482=
ENST00000467558.5:n.2818C>G
ENST00000469750.5:n.4018C>G
ENST00000473879.1:n.162C>G
ENST00000493232.5:n.4182C>G
NM_152743.3:c.1446C>G	NP_689956.2:p.Pro482=
XM_005249643.3:c.1446C>G	XP_005249700.1:p.Pro482=
XM_011515177.1:c.1530C>G	XP_011513479.1:p.Pro510=
XM_011515178.1:c.1530C>G	XP_011513480.1:p.Pro510=
XM_011515179.1:c.1527C>G	XP_011513481.1:p.Pro509=
XM_011515180.1:c.1500C>G	XP_011513482.1:p.Pro500=
XM_011515181.1:c.1530C>G	XP_011513483.1:p.Pro510=
XM_011515182.1:c.1530C>G	XP_011513484.1:p.Pro510=
XM_011515183.1:c.1005C>G	XP_011513485.1:p.Pro335=
XM_011515184.1:c.1005C>G	XP_011513486.1:p.Pro335=
XM_011515185.1:c.1446C>G	XP_011513487.1:p.Pro482=
XM_011515186.1:c.1530C>G	XP_011513488.1:p.Pro510=
XM_011515187.1:c.102C>G	XP_011513489.1:p.Pro34=
NM_001350626.1:c.1446C>G	NP_001337555.1:p.Pro482=
NM_001350627.1:c.921C>G	NP_001337556.1:p.Pro307=
NR_146879.1:n.1863C>G
XM_011515177.2:c.1530C>G	XP_011513479.1:p.Pro510=
XM_011515179.2:c.1527C>G	XP_011513481.1:p.Pro509=
XM_011515181.2:c.1530C>G	XP_011513483.1:p.Pro510=
XM_011515182.2:c.1530C>G	XP_011513484.1:p.Pro510=
XM_011515184.3:c.1005C>G	XP_011513486.1:p.Pro335=
XM_011515186.2:c.1530C>G	XP_011513488.1:p.Pro510=
XM_017011833.1:c.1443C>G	XP_016867322.1:p.Pro481=
XM_017011834.1:c.1443C>G	XP_016867323.1:p.Pro481=
XM_017011836.2:c.1446C>G	XP_016867325.1:p.Pro482=
XM_024446682.1:c.102C>G	XP_024302450.1:p.Pro34=
NM_152743.4:c.1446C>G MANE Select	NP_689956.2:p.Pro482=
NM_001350626.2:c.1446C>G	NP_001337555.1:p.Pro482=
NM_001350627.2:c.921C>G	NP_001337556.1:p.Pro307=
NR_146879.2:n.1629C>G