Allele Registry

Canonical Allele Identifier: CA130211

Gene: GNRHR HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr4:g.67754305_67754306delinsTT

GRCh37 chr4:g.68620023_68620024delinsTT

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000030919

RCV000498552

ClinVar Variation:

189195

dbSNP:

281865427

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754305_67754306delinsTT , CM000666.2:g.67754305_67754306delinsTT	GRCh38
NC_000004.11:g.68620023_68620024delinsTT , CM000666.1:g.68620023_68620024delinsTT	GRCh37
NC_000004.10:g.68302618_68302619delinsTT	NCBI36
NG_009293.1:g.6781_6782delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.30_31delinsAA MANE Select	ENSP00000226413.5:p.Asn10_Gln11delinsLysLys
ENST00000226413.4:c.30_31delinsAA	ENSP00000226413.4:p.Asn10_Gln11delinsLysLys
ENST00000420975.2:c.30_31delinsAA	ENSP00000397561.2:p.Asn10_Gln11delinsLysLys
NM_000406.2:c.30_31delinsAA	NP_000397.1:p.Asn10_Gln11delinsLysLys
NM_001012763.1:c.30_31delinsAA	NP_001012781.1:p.Asn10_Gln11delinsLysLys
NM_000406.3:c.30_31delinsAA MANE Select	NP_000397.1:p.Asn10_Gln11delinsLysLys
NM_001012763.2:c.30_31delinsAA	NP_001012781.1:p.Asn10_Gln11delinsLysLys

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