Canonical Allele Identifier: CA1905675910
Gene: BMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.42798120T= , CM000672.2:g.42798120T= GRCh38
NC_000010.10:g.43293568T= , CM000672.1:g.43293568T= GRCh37
NC_000010.9:g.42613574T= NCBI36
NG_046921.1:g.20615T=

Transcript Alleles

HGVS Amino-acid change
ENST00000374518.6:c.2090-348T= MANE Select ENSP00000363642.4:n.2090-348T=
ENST00000374518.5:c.2090-348T= ENSP00000363642.4:n.2090-348T=
NM_014753.3:c.2090-348T= NP_055568.3:n.2090-348T=
XM_005271846.2:c.2090-348T= XP_005271903.1:n.2090-348T=
XM_005271847.2:c.1901-348T= XP_005271904.1:n.1901-348T=
XM_005271848.2:c.2090-348T= XP_005271905.1:n.2090-348T=
XM_005271849.2:c.2090-348T= XP_005271906.1:n.2090-348T=
XM_006718081.2:c.2090-348T= XP_006718144.1:n.2090-348T=
XM_011540402.1:c.2090-348T= XP_011538704.1:n.2090-348T=
XM_011540403.1:c.857-348T= XP_011538705.1:n.857-348T=
XR_246522.1:n.2179-348T=
XR_428728.2:n.2179-348T=
XM_005271846.3:c.2090-348T= XP_005271903.1:n.2090-348T=
XM_005271848.3:c.2090-348T= XP_005271905.1:n.2090-348T=
XM_011540402.2:c.2090-348T= XP_011538704.1:n.2090-348T=
XM_011540403.2:c.857-348T= XP_011538705.1:n.857-348T=
XR_001747266.1:n.2179-348T=
XR_002957049.1:n.2179-348T=
NM_014753.4:c.2090-348T= MANE Select NP_055568.3:n.2090-348T=