Canonical Allele Identifier: CA366625494

Gene: BRAT1

Linked Data

• MyVariant Identifiers: chr7:g.2578323A>C (hg19) ; chr7:g.2538689A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2538689A>C , CM000669.2:g.2538689A>C	GRCh38
NC_000007.13:g.2578323A>C , CM000669.1:g.2578323A>C	GRCh37
NC_000007.12:g.2544849A>C	NCBI36
NG_032167.1:g.22070T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340611.9:c.1846T>G MANE Select	ENSP00000339637.4:p.Phe616Val
ENST00000340611.8:c.1846T>G	ENSP00000339637.4:p.Phe616Val
ENST00000467558.5:n.3632T>G
ENST00000469750.5:n.4418T>G
ENST00000473879.1:n.389T>G
ENST00000493232.5:n.4552T>G
NM_152743.3:c.1846T>G	NP_689956.2:p.Phe616Val
XM_005249643.3:c.2026T>G	XP_005249700.1:p.Phe676Val
XM_011515177.1:c.2110T>G	XP_011513479.1:p.Phe704Val
XM_011515178.1:c.2110T>G	XP_011513480.1:p.Phe704Val
XM_011515179.1:c.2107T>G	XP_011513481.1:p.Phe703Val
XM_011515180.1:c.2080T>G	XP_011513482.1:p.Phe694Val
XM_011515181.1:c.1930T>G	XP_011513483.1:p.Phe644Val
XM_011515182.1:c.2110T>G	XP_011513484.1:p.Phe704Val
XM_011515183.1:c.1585T>G	XP_011513485.1:p.Phe529Val
XM_011515184.1:c.1585T>G	XP_011513486.1:p.Phe529Val
XM_011515185.1:c.1846T>G	XP_011513487.1:p.Phe616Val
XM_011515186.1:c.1757T>G	XP_011513488.1:p.Leu586Arg
XM_011515187.1:c.682T>G	XP_011513489.1:p.Phe228Val
NM_001350626.1:c.2026T>G	NP_001337555.1:p.Phe676Val
NM_001350627.1:c.1321T>G	NP_001337556.1:p.Phe441Val
NR_146879.1:n.2263T>G
XM_011515177.2:c.2110T>G	XP_011513479.1:p.Phe704Val
XM_011515179.2:c.2107T>G	XP_011513481.1:p.Phe703Val
XM_011515181.2:c.1930T>G	XP_011513483.1:p.Phe644Val
XM_011515182.2:c.2110T>G	XP_011513484.1:p.Phe704Val
XM_011515184.3:c.1585T>G	XP_011513486.1:p.Phe529Val
XM_011515186.2:c.1757T>G	XP_011513488.1:p.Leu586Arg
XM_017011833.1:c.2023T>G	XP_016867322.1:p.Phe675Val
XM_017011834.1:c.1843T>G	XP_016867323.1:p.Phe615Val
XM_017011836.2:c.1673T>G	XP_016867325.1:p.Leu558Arg
XM_024446682.1:c.682T>G	XP_024302450.1:p.Phe228Val
NM_152743.4:c.1846T>G MANE Select	NP_689956.2:p.Phe616Val
NM_001350626.2:c.2026T>G	NP_001337555.1:p.Phe676Val
NM_001350627.2:c.1321T>G	NP_001337556.1:p.Phe441Val
NR_146879.2:n.2029T>G