Canonical Allele Identifier: CA1557931488
Gene: HOMER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79460955T= , CM000667.2:g.79460955T= GRCh38
NC_000005.9:g.78756778T= , CM000667.1:g.78756778T= GRCh37
NC_000005.8:g.78792534T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_004272.5:c.6-3937A= MANE Select NP_004263.1:n.6-3937A=
ENST00000334082.11:c.6-3937A= MANE Select ENSP00000334382.6:n.6-3937A=
NM_001277077.1:c.6-3937A= NP_001264006.1:n.6-3937A=
NM_001277078.1:c.6-3937A= NP_001264007.1:n.6-3937A=
NM_004272.4:c.6-3937A= NP_004263.1:n.6-3937A=
ENST00000282260.10:c.6-3937A= ENSP00000282260.6:n.6-3937A=
ENST00000334082.10:c.6-3937A= ENSP00000334382.6:n.6-3937A=
ENST00000508576.5:c.6-3937A= ENSP00000426651.1:n.6-3937A=
ENST00000535690.1:c.5+51815A= ENSP00000441587.1:n.5+51815A=
XM_017010059.2:c.6-3937A= XP_016865548.1:n.6-3937A=