Canonical Allele Identifier: CA2938975
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs767948707
ExAC: 4:68619855 TCTTCTGTGTCCA / T
gnomAD v2: 4-68619855-TCTTCTGTGTCCA-T
gnomAD v4: 4-67754137-TCTTCTGTGTCCA-T
MyVariant Identifiers: chr4:g.68619856_68619867del (hg19) chr4:g.67754138_67754149del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754144_67754155del , CM000666.2:g.67754144_67754155del GRCh38
NC_000004.11:g.68619862_68619873del , CM000666.1:g.68619862_68619873del GRCh37
NC_000004.10:g.68302457_68302468del NCBI36
NG_009293.1:g.6938_6949del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.187_198del MANE Select ENSP00000226413.5:p.Trp63_Lys66del
ENST00000226413.4:c.187_198del ENSP00000226413.4:p.Trp63_Lys66del
ENST00000420975.2:c.187_198del ENSP00000397561.2:p.Trp63_Lys66del
NM_000406.2:c.187_198del NP_000397.1:p.Trp63_Lys66del
NM_001012763.1:c.187_198del NP_001012781.1:p.Trp63_Lys66del
NM_000406.3:c.187_198del MANE Select NP_000397.1:p.Trp63_Lys66del
NM_001012763.2:c.187_198del NP_001012781.1:p.Trp63_Lys66del
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