Canonical Allele Identifier: CA366628170

Gene: BRAT1

Linked Data

• MyVariant Identifiers: chr7:g.2579450G>C (hg19) ; chr7:g.2539816G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2539816G>C , CM000669.2:g.2539816G>C	GRCh38
NC_000007.13:g.2579450G>C , CM000669.1:g.2579450G>C	GRCh37
NC_000007.12:g.2545976G>C	NCBI36
NG_032167.1:g.20943C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340611.9:c.1468C>G MANE Select	ENSP00000339637.4:p.Leu490Val
ENST00000340611.8:c.1468C>G	ENSP00000339637.4:p.Leu490Val
ENST00000467558.5:n.2840C>G
ENST00000469750.5:n.4040C>G
ENST00000473879.1:n.184C>G
ENST00000493232.5:n.4204C>G
NM_152743.3:c.1468C>G	NP_689956.2:p.Leu490Val
XM_005249643.3:c.1468C>G	XP_005249700.1:p.Leu490Val
XM_011515177.1:c.1552C>G	XP_011513479.1:p.Leu518Val
XM_011515178.1:c.1552C>G	XP_011513480.1:p.Leu518Val
XM_011515179.1:c.1549C>G	XP_011513481.1:p.Leu517Val
XM_011515180.1:c.1522C>G	XP_011513482.1:p.Leu508Val
XM_011515181.1:c.1552C>G	XP_011513483.1:p.Leu518Val
XM_011515182.1:c.1552C>G	XP_011513484.1:p.Leu518Val
XM_011515183.1:c.1027C>G	XP_011513485.1:p.Leu343Val
XM_011515184.1:c.1027C>G	XP_011513486.1:p.Leu343Val
XM_011515185.1:c.1468C>G	XP_011513487.1:p.Leu490Val
XM_011515186.1:c.1552C>G	XP_011513488.1:p.Leu518Val
XM_011515187.1:c.124C>G	XP_011513489.1:p.Leu42Val
NM_001350626.1:c.1468C>G	NP_001337555.1:p.Leu490Val
NM_001350627.1:c.943C>G	NP_001337556.1:p.Leu315Val
NR_146879.1:n.1885C>G
XM_011515177.2:c.1552C>G	XP_011513479.1:p.Leu518Val
XM_011515179.2:c.1549C>G	XP_011513481.1:p.Leu517Val
XM_011515181.2:c.1552C>G	XP_011513483.1:p.Leu518Val
XM_011515182.2:c.1552C>G	XP_011513484.1:p.Leu518Val
XM_011515184.3:c.1027C>G	XP_011513486.1:p.Leu343Val
XM_011515186.2:c.1552C>G	XP_011513488.1:p.Leu518Val
XM_017011833.1:c.1465C>G	XP_016867322.1:p.Leu489Val
XM_017011834.1:c.1465C>G	XP_016867323.1:p.Leu489Val
XM_017011836.2:c.1468C>G	XP_016867325.1:p.Leu490Val
XM_024446682.1:c.124C>G	XP_024302450.1:p.Leu42Val
NM_152743.4:c.1468C>G MANE Select	NP_689956.2:p.Leu490Val
NM_001350626.2:c.1468C>G	NP_001337555.1:p.Leu490Val
NM_001350627.2:c.943C>G	NP_001337556.1:p.Leu315Val
NR_146879.2:n.1651C>G