Canonical Allele Identifier: CA1622225698
Gene: BTBD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38398016G= , CM000668.2:g.38398016G= GRCh38
NC_000006.11:g.38365792G= , CM000668.1:g.38365792G= GRCh37
NC_000006.10:g.38473770G= NCBI36
NG_016545.1:g.247133C=

Transcript Alleles

HGVS Amino-acid change
ENST00000481247.6:c.1155-52923C= MANE Select ENSP00000418751.1:n.1155-52923C=
ENST00000649492.1:c.1155-52923C= ENSP00000497066.1:n.1155-52923C=
ENST00000314100.10:c.951-52923C= ENSP00000323408.6:n.951-52923C=
ENST00000328403.10:c.*63-52923C= ENSP00000328328.6:n.*63-52923C=
ENST00000419706.6:c.1064+4801C= ENSP00000415365.2:n.1064+4801C=
ENST00000481247.5:c.1155-52923C= ENSP00000418751.1:n.1155-52923C=
NM_001099272.1:c.1155-52923C= NP_001092742.1:n.1155-52923C=
NM_001172418.1:c.1064+4801C= NP_001165889.1:n.1064+4801C=
NM_052893.1:c.1155-52923C= NP_443125.1:n.1155-52923C=
NM_152733.2:c.951-52923C= NP_689946.2:n.951-52923C=
XM_005248841.2:c.1155-52923C= XP_005248898.1:n.1155-52923C=
XM_011514279.1:c.1155-52923C= XP_011512581.1:n.1155-52923C=
XM_011514281.1:c.1155-52746C= XP_011512583.1:n.1155-52746C=
XM_011514279.3:c.1155-52923C= XP_011512581.1:n.1155-52923C=
XM_011514281.3:c.1155-52746C= XP_011512583.1:n.1155-52746C=
NM_001099272.2:c.1155-52923C= MANE Select NP_001092742.1:n.1155-52923C=
NM_052893.2:c.1155-52923C= NP_443125.1:n.1155-52923C=
NM_001172418.2:c.1064+4801C= NP_001165889.1:n.1064+4801C=
NM_152733.3:c.951-52923C= NP_689946.2:n.951-52923C=