Canonical Allele Identifier: CA341073456
Gene: BRDT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91962944C>G , CM000663.2:g.91962944C>G GRCh38
NC_000001.10:g.92428501C>G , CM000663.1:g.92428501C>G GRCh37
NC_000001.9:g.92201089C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000399546.7:c.190C>G MANE Select ENSP00000387822.3:p.Pro64Ala
ENST00000426141.6:c.190C>G ENSP00000404969.1:p.Pro64Ala
ENST00000448194.6:c.190C>G ENSP00000410587.2:p.Pro64Ala
ENST00000470955.6:c.190C>G ENSP00000506247.1:p.Pro64Ala
ENST00000680091.1:c.232C>G ENSP00000506227.1:p.Pro78Ala
ENST00000680541.1:c.-21-5202C>G ENSP00000505035.1:n.-21-5202C>G
ENST00000362005.7:c.190C>G ENSP00000354568.3:p.Pro64Ala
ENST00000370389.6:c.-27-1683C>G ENSP00000359416.2:n.-27-1683C>G
ENST00000394530.7:c.190C>G ENSP00000378038.3:p.Pro64Ala
ENST00000399546.6:c.190C>G ENSP00000387822.2:p.Pro64Ala
ENST00000402388.1:c.190C>G ENSP00000384051.1:p.Pro64Ala
ENST00000423434.5:c.190C>G ENSP00000396351.1:p.Pro64Ala
ENST00000426141.5:c.190C>G ENSP00000404969.1:p.Pro64Ala
ENST00000427104.5:c.190C>G ENSP00000400002.1:p.Pro64Ala
ENST00000440509.5:c.190C>G ENSP00000416714.1:p.Pro64Ala
ENST00000448194.5:c.190C>G ENSP00000410587.1:p.Pro64Ala
ENST00000450792.5:c.190C>G ENSP00000414349.1:p.Pro64Ala
ENST00000548992.5:c.190C>G ENSP00000447394.1:p.Pro64Ala
ENST00000552654.1:c.-30C>G ENSP00000446599.1:n.-30C>G
NM_001242805.2:c.190C>G NP_001229734.2:p.Pro64Ala
NM_001242806.2:c.190C>G NP_001229735.2:p.Pro64Ala
NM_001242807.2:c.190C>G NP_001229736.2:p.Pro64Ala
NM_001242808.2:c.190C>G NP_001229737.2:p.Pro64Ala
NM_001242810.2:c.-27-1683C>G NP_001229739.2:n.-27-1683C>G
NM_001726.4:c.190C>G NP_001717.3:p.Pro64Ala
NM_207189.3:c.190C>G NP_997072.2:p.Pro64Ala
XM_006710853.2:c.190C>G XP_006710916.1:p.Pro64Ala
XM_006710854.2:c.190C>G XP_006710917.1:p.Pro64Ala
XM_006710855.2:c.190C>G XP_006710918.1:p.Pro64Ala
XM_006710856.2:c.190C>G XP_006710919.1:p.Pro64Ala
XM_006710857.2:c.190C>G XP_006710920.1:p.Pro64Ala
XM_011542032.1:c.190C>G XP_011540334.1:p.Pro64Ala
XM_011542033.1:c.190C>G XP_011540335.1:p.Pro64Ala
XM_011542034.1:c.190C>G XP_011540336.1:p.Pro64Ala
XM_011542035.1:c.190C>G XP_011540337.1:p.Pro64Ala
XM_011542036.1:c.190C>G XP_011540338.1:p.Pro64Ala
XM_006710853.4:c.190C>G XP_006710916.1:p.Pro64Ala
XM_006710854.4:c.190C>G XP_006710917.1:p.Pro64Ala
XM_006710855.4:c.190C>G XP_006710918.1:p.Pro64Ala
XM_006710856.4:c.190C>G XP_006710919.1:p.Pro64Ala
XM_006710857.4:c.190C>G XP_006710920.1:p.Pro64Ala
XM_011542032.3:c.190C>G XP_011540334.1:p.Pro64Ala
XM_011542033.3:c.190C>G XP_011540335.1:p.Pro64Ala
XM_011542034.3:c.190C>G XP_011540336.1:p.Pro64Ala
XM_011542035.3:c.190C>G XP_011540337.1:p.Pro64Ala
XM_011542036.3:c.190C>G XP_011540338.1:p.Pro64Ala
NM_207189.4:c.190C>G MANE Select NP_997072.2:p.Pro64Ala