Canonical Allele Identifier: CA1683199354

Gene: BRAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2539876_2539879delinsCCTT , CM000669.2:g.2539876_2539879delinsCCTT	GRCh38
NC_000007.13:g.2579510_2579513delinsCCTT , CM000669.1:g.2579510_2579513delinsCCTT	GRCh37
NC_000007.12:g.2546036_2546039delinsCCTT	NCBI36
NG_032167.1:g.20880_20883delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340611.9:c.1405_1408delinsAAGG MANE Select	ENSP00000339637.4:p.Lys469=
ENST00000340611.8:c.1405_1408delinsAAGG	ENSP00000339637.4:p.Lys469=
ENST00000467558.5:n.2777_2780delinsAAGG
ENST00000469750.5:n.3977_3980delinsAAGG
ENST00000473879.1:n.121_124delinsAAGG
ENST00000493232.5:n.4141_4144delinsAAGG
NM_152743.3:c.1405_1408delinsAAGG	NP_689956.2:p.Lys469=
XM_005249643.3:c.1405_1408delinsAAGG	XP_005249700.1:p.Lys469=
XM_011515177.1:c.1489_1492delinsAAGG	XP_011513479.1:p.Lys497=
XM_011515178.1:c.1489_1492delinsAAGG	XP_011513480.1:p.Lys497=
XM_011515179.1:c.1486_1489delinsAAGG	XP_011513481.1:p.Lys496=
XM_011515180.1:c.1459_1462delinsAAGG	XP_011513482.1:p.Lys487=
XM_011515181.1:c.1489_1492delinsAAGG	XP_011513483.1:p.Lys497=
XM_011515182.1:c.1489_1492delinsAAGG	XP_011513484.1:p.Lys497=
XM_011515183.1:c.964_967delinsAAGG	XP_011513485.1:p.Lys322=
XM_011515184.1:c.964_967delinsAAGG	XP_011513486.1:p.Lys322=
XM_011515185.1:c.1405_1408delinsAAGG	XP_011513487.1:p.Lys469=
XM_011515186.1:c.1489_1492delinsAAGG	XP_011513488.1:p.Lys497=
XM_011515187.1:c.61_64delinsAAGG	XP_011513489.1:p.Lys21=
NM_001350626.1:c.1405_1408delinsAAGG	NP_001337555.1:p.Lys469=
NM_001350627.1:c.880_883delinsAAGG	NP_001337556.1:p.Lys294=
NR_146879.1:n.1822_1825delinsAAGG
XM_011515177.2:c.1489_1492delinsAAGG	XP_011513479.1:p.Lys497=
XM_011515179.2:c.1486_1489delinsAAGG	XP_011513481.1:p.Lys496=
XM_011515181.2:c.1489_1492delinsAAGG	XP_011513483.1:p.Lys497=
XM_011515182.2:c.1489_1492delinsAAGG	XP_011513484.1:p.Lys497=
XM_011515184.3:c.964_967delinsAAGG	XP_011513486.1:p.Lys322=
XM_011515186.2:c.1489_1492delinsAAGG	XP_011513488.1:p.Lys497=
XM_017011833.1:c.1402_1405delinsAAGG	XP_016867322.1:p.Lys468=
XM_017011834.1:c.1402_1405delinsAAGG	XP_016867323.1:p.Lys468=
XM_017011836.2:c.1405_1408delinsAAGG	XP_016867325.1:p.Lys469=
XM_024446682.1:c.61_64delinsAAGG	XP_024302450.1:p.Lys21=
NM_152743.4:c.1405_1408delinsAAGG MANE Select	NP_689956.2:p.Lys469=
NM_001350626.2:c.1405_1408delinsAAGG	NP_001337555.1:p.Lys469=
NM_001350627.2:c.880_883delinsAAGG	NP_001337556.1:p.Lys294=
NR_146879.2:n.1588_1591delinsAAGG