Canonical Allele Identifier: CA214411071
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs934428390
gnomAD v2: 10-124265964-GGT-G
gnomAD v3: 10-122506448-GGT-G
gnomAD v4: 10-122506448-GGT-G
MyVariant Identifiers: chr10:g.124265965_124265966del (hg19) chr10:g.122506449_122506450del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506458_122506459del , CM000672.2:g.122506458_122506459del GRCh38
NC_000010.10:g.124265974_124265975del , CM000672.1:g.124265974_124265975del GRCh37
NC_000010.9:g.124255964_124255965del NCBI36
NG_011554.1:g.49934_49935del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.778-233_778-232del MANE Select ENSP00000357980.3:n.778-233_778-232del
ENST00000648167.1:c.460-233_460-232del ENSP00000498033.1:n.460-233_460-232del
ENST00000368984.7:c.778-233_778-232del ENSP00000357980.3:n.778-233_778-232del
NM_002775.4:c.778-233_778-232del NP_002766.1:n.778-233_778-232del
NM_002775.5:c.778-233_778-232del MANE Select NP_002766.1:n.778-233_778-232del
Search 100 bp 5'
Search 100 bp 3'