Canonical Allele Identifier: CA451355798
Gene: HTR1E HGNC NCBI

Linked Data

COSMIC: COSM1446246
MyVariant Identifiers: chr6:g.87725557del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015843del , CM000668.2:g.87015843del GRCh38
NC_000006.11:g.87725561del , CM000668.1:g.87725561del GRCh37
NC_000006.10:g.87782280del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.509del MANE Select ENSP00000307766.4:p.Pro170LeufsTer26
ENST00000305344.6:c.509del ENSP00000307766.4:p.Pro170LeufsTer26
NM_000865.2:c.509del NP_000856.1:p.Pro170LeufsTer26
XM_011535789.1:c.509del XP_011534091.1:p.Pro170LeufsTer26
XM_011535790.1:c.509del XP_011534092.1:p.Pro170LeufsTer26
XM_011535789.2:c.509del XP_011534091.1:p.Pro170LeufsTer26
NM_000865.3:c.509del MANE Select NP_000856.1:p.Pro170LeufsTer26
Search 100 bp 5'
Search 100 bp 3'