Canonical Allele Identifier: CA14954715
Gene: BRD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49824963A>C , CM000684.2:g.49824963A>C GRCh38
NC_000022.10:g.50218611A>C , CM000684.1:g.50218611A>C GRCh37
NC_000022.9:g.48604615A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404760.6:c.-14-632T>G MANE Select ENSP00000385858.1:n.-14-632T>G
ENST00000404034.5:c.-14-632T>G ENSP00000384076.1:n.-14-632T>G
ENST00000404760.5:c.-14-632T>G ENSP00000385858.1:n.-14-632T>G
NM_001304808.1:c.-14-632T>G NP_001291737.1:n.-14-632T>G
NM_001304809.1:c.-14-632T>G NP_001291738.1:n.-14-632T>G
XM_011530064.1:c.-14-632T>G XP_011528366.1:n.-14-632T>G
XM_011530069.1:c.-14-632T>G XP_011528371.1:n.-14-632T>G
XM_011530071.1:c.-14-632T>G XP_011528373.1:n.-14-632T>G
XR_244360.1:n.53-632T>G
NM_001304808.2:c.-14-632T>G NP_001291737.1:n.-14-632T>G
XM_017028715.1:c.-14-632T>G XP_016884204.1:n.-14-632T>G
XM_017028716.1:c.-14-632T>G XP_016884205.1:n.-14-632T>G
NM_001304808.3:c.-14-632T>G MANE Select NP_001291737.1:n.-14-632T>G
NM_001349940.2:c.-14-632T>G NP_001336869.1:n.-14-632T>G
NM_001349941.2:c.-14-632T>G NP_001336870.1:n.-14-632T>G
NM_001349942.2:c.-1709-632T>G NP_001336871.1:n.-1709-632T>G
NM_001394548.1:c.-14-632T>G NP_001381477.1:n.-14-632T>G
NM_001394549.1:c.-14-632T>G NP_001381478.1:n.-14-632T>G
NM_001394550.1:c.-176+2534T>G NP_001381479.1:n.-176+2534T>G
NM_001394551.1:c.-14-632T>G NP_001381480.1:n.-14-632T>G
NM_001394552.1:c.-646T>G NP_001381481.1:n.-646T>G
NR_146334.2:n.378-632T>G
NR_146335.2:n.378-632T>G
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