Canonical Allele Identifier: CA1465421047

Gene: GNRHR

Linked Data

• dbSNP Id: rs1731932315

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754383_67754384insTGT , CM000666.2:g.67754383_67754384insTGT	GRCh38
NC_000004.11:g.68620101_68620102insTGT , CM000666.1:g.68620101_68620102insTGT	GRCh37
NC_000004.10:g.68302696_68302697insTGT	NCBI36
NG_009293.1:g.6704_6705insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.-48_-47insCAA MANE Select	ENSP00000226413.5:n.-48_-47insCAA
NM_000406.2:c.-48_-47insCAA	NP_000397.1:n.-48_-47insCAA
NM_001012763.1:c.-48_-47insCAA	NP_001012781.1:n.-48_-47insCAA
NM_000406.3:c.-48_-47insCAA MANE Select	NP_000397.1:n.-48_-47insCAA
NM_001012763.2:c.-48_-47insCAA	NP_001012781.1:n.-48_-47insCAA