Canonical Allele Identifier: CA366625488

Gene: BRAT1

Linked Data

• MyVariant Identifiers: chr7:g.2578321G>C (hg19) ; chr7:g.2538687G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2538687G>C , CM000669.2:g.2538687G>C	GRCh38
NC_000007.13:g.2578321G>C , CM000669.1:g.2578321G>C	GRCh37
NC_000007.12:g.2544847G>C	NCBI36
NG_032167.1:g.22072C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000340611.9:c.1848C>G MANE Select	ENSP00000339637.4:p.Phe616Leu
ENST00000340611.8:c.1848C>G	ENSP00000339637.4:p.Phe616Leu
ENST00000467558.5:n.3634C>G
ENST00000469750.5:n.4420C>G
ENST00000473879.1:n.391C>G
ENST00000493232.5:n.4554C>G
NM_152743.3:c.1848C>G	NP_689956.2:p.Phe616Leu
XM_005249643.3:c.2028C>G	XP_005249700.1:p.Phe676Leu
XM_011515177.1:c.2112C>G	XP_011513479.1:p.Phe704Leu
XM_011515178.1:c.2112C>G	XP_011513480.1:p.Phe704Leu
XM_011515179.1:c.2109C>G	XP_011513481.1:p.Phe703Leu
XM_011515180.1:c.2082C>G	XP_011513482.1:p.Phe694Leu
XM_011515181.1:c.1932C>G	XP_011513483.1:p.Phe644Leu
XM_011515182.1:c.2112C>G	XP_011513484.1:p.Phe704Leu
XM_011515183.1:c.1587C>G	XP_011513485.1:p.Phe529Leu
XM_011515184.1:c.1587C>G	XP_011513486.1:p.Phe529Leu
XM_011515185.1:c.1848C>G	XP_011513487.1:p.Phe616Leu
XM_011515186.1:c.1759C>G	XP_011513488.1:p.His587Asp
XM_011515187.1:c.684C>G	XP_011513489.1:p.Phe228Leu
NM_001350626.1:c.2028C>G	NP_001337555.1:p.Phe676Leu
NM_001350627.1:c.1323C>G	NP_001337556.1:p.Phe441Leu
NR_146879.1:n.2265C>G
XM_011515177.2:c.2112C>G	XP_011513479.1:p.Phe704Leu
XM_011515179.2:c.2109C>G	XP_011513481.1:p.Phe703Leu
XM_011515181.2:c.1932C>G	XP_011513483.1:p.Phe644Leu
XM_011515182.2:c.2112C>G	XP_011513484.1:p.Phe704Leu
XM_011515184.3:c.1587C>G	XP_011513486.1:p.Phe529Leu
XM_011515186.2:c.1759C>G	XP_011513488.1:p.His587Asp
XM_017011833.1:c.2025C>G	XP_016867322.1:p.Phe675Leu
XM_017011834.1:c.1845C>G	XP_016867323.1:p.Phe615Leu
XM_017011836.2:c.1675C>G	XP_016867325.1:p.His559Asp
XM_024446682.1:c.684C>G	XP_024302450.1:p.Phe228Leu
NM_152743.4:c.1848C>G MANE Select	NP_689956.2:p.Phe616Leu
NM_001350626.2:c.2028C>G	NP_001337555.1:p.Phe676Leu
NM_001350627.2:c.1323C>G	NP_001337556.1:p.Phe441Leu
NR_146879.2:n.2031C>G