Canonical Allele Identifier: CA10627552

Gene: GNRH1

Linked Data

• ClinVar Variation Id: 362660
• ClinVar RCV Id: RCV000400073
• dbSNP Id: rs71551806
• gnomAD v2: 8-25281872-C-CT
• gnomAD v3: 8-25424356-C-CT
• gnomAD v4: 8-25424356-C-CT
• COSMIC: COSN20105308 ; COSN20105309 ; COSN20105310 ; COSN20105311
• MyVariant Identifiers: chr8:g.25281873dupT (hg19) ; chr8:g.25281873_25281874insT (hg19) ; chr8:g.25281872_25281873insT (hg19) ; chr8:g.25424357dupT (hg38) ; chr8:g.25424357_25424358insT (hg38) ; chr8:g.25424356_25424357insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.25424368dup , CM000670.2:g.25424368dup	GRCh38
NC_000008.10:g.25281884dup , CM000670.1:g.25281884dup	GRCh37
NC_000008.9:g.25337801dup	NCBI36
NG_016457.1:g.5684dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276414.4:c.-1027dup	ENSP00000276414.4:n.-1027dup
NM_000825.3:c.-1015dup	NP_000816.4:n.-1015dup
NM_001083111.1:c.-158dup	NP_001076580.1:n.-158dup