Canonical Allele Identifier: CA1557931489
Gene: HOMER1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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