Canonical Allele Identifier: CA2673999501
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63962188-CTCCTCCTCTCTTCTCTCTCTTCTGCCTCTTTCGTCCCCCTTCTCCCCACCTGCCTTCCCTTTCAGTCTCCCTCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962197_63962270del , CM000667.2:g.63962197_63962270del GRCh38
NC_000005.9:g.63258024_63258097del , CM000667.1:g.63258024_63258097del GRCh37
NC_000005.8:g.63293780_63293853del NCBI36
NG_032816.1:g.5031_5104del

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-543_-470del MANE Select ENSP00000316244.4:n.-543_-470del
ENST00000506598.1:c.-387-156_-387-83del ENSP00000423433.1:n.-387-156_-387-83del
NM_000524.3:c.-543_-470del NP_000515.2:n.-543_-470del
NM_000524.4:c.-543_-470del MANE Select NP_000515.2:n.-543_-470del
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