Canonical Allele Identifier: CA1644352379
Gene: HTR1E HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015835C= , CM000668.2:g.87015835C= GRCh38
NC_000006.11:g.87725553C= , CM000668.1:g.87725553C= GRCh37
NC_000006.10:g.87782272C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.501C= MANE Select ENSP00000307766.4:p.Ser167=
ENST00000305344.6:c.501C= ENSP00000307766.4:p.Ser167=
NM_000865.2:c.501C= NP_000856.1:p.Ser167=
XM_011535789.1:c.501C= XP_011534091.1:p.Ser167=
XM_011535790.1:c.501C= XP_011534092.1:p.Ser167=
XM_011535789.2:c.501C= XP_011534091.1:p.Ser167=
NM_000865.3:c.501C= MANE Select NP_000856.1:p.Ser167=
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