Canonical Allele Identifier: CA1345152264

Gene: GHRL GHRLOS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10289884_10289885delinsAG , CM000665.2:g.10289884_10289885delinsAG	GRCh38
NC_000003.11:g.10331568_10331569delinsAG , CM000665.1:g.10331568_10331569delinsAG	GRCh37
NC_000003.10:g.10306568_10306569delinsAG	NCBI36
NG_011560.1:g.8063_8064delinsCT
NG_033090.1:g.13933_13934delinsAG
NG_033090.2:g.13933_13934delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335542.13:c.109-7_109-6delinsCT (GHRL) MANE Select	ENSP00000335074.8:n.109-7_109-6delinsCT
ENST00000287656.11:c.109-10_109-9delinsCT (GHRL)	ENSP00000287656.7:n.109-10_109-9delinsCT
ENST00000335542.12:c.109-7_109-6delinsCT (GHRL)	ENSP00000335074.8:n.109-7_109-6delinsCT
ENST00000422159.5:c.109-7_109-6delinsCT (GHRL)	ENSP00000405464.1:n.109-7_109-6delinsCT
ENST00000429122.1:c.109-7_109-6delinsCT (GHRL)	ENSP00000414819.1:n.109-7_109-6delinsCT
ENST00000430179.5:c.109-10_109-9delinsCT (GHRL)	ENSP00000399922.1:n.109-10_109-9delinsCT
ENST00000437422.6:c.73-7_73-6delinsCT (GHRL)	ENSP00000416768.2:n.73-7_73-6delinsCT
ENST00000439975.6:c.72+2957_72+2958delinsCT (GHRL)	ENSP00000403725.2:n.72+2957_72+2958delinsCT
ENST00000446937.2:c.72+2957_72+2958delinsCT (GHRL)	ENSP00000394923.2:n.72+2957_72+2958delinsCT
ENST00000449238.6:c.73-10_73-9delinsCT (GHRL)	ENSP00000388145.2:n.73-10_73-9delinsCT
ENST00000457360.5:c.109-7_109-6delinsCT (GHRL)	ENSP00000391406.1:n.109-7_109-6delinsCT
ENST00000481287.5:n.286-7_286-6delinsCT (GHRL)
ENST00000491589.5:n.200-7_200-6delinsCT (GHRL)
NM_001134941.2:c.109-10_109-9delinsCT (GHRL)	NP_001128413.1:n.109-10_109-9delinsCT
NM_001134944.1:c.73-7_73-6delinsCT (GHRL)	NP_001128416.1:n.73-7_73-6delinsCT
NM_001134945.1:c.73-10_73-9delinsCT (GHRL)	NP_001128417.1:n.73-10_73-9delinsCT
NM_001134946.1:c.72+2957_72+2958delinsCT (GHRL)	NP_001128418.1:n.72+2957_72+2958delinsCT
NM_001302821.1:c.109-7_109-6delinsCT (GHRL)	NP_001289750.1:n.109-7_109-6delinsCT
NM_001302822.1:c.109-7_109-6delinsCT (GHRL)	NP_001289751.1:n.109-7_109-6delinsCT
NM_001302823.1:c.109-10_109-9delinsCT (GHRL)	NP_001289752.1:n.109-10_109-9delinsCT
NM_001302824.1:c.109-7_109-6delinsCT (GHRL)	NP_001289753.1:n.109-7_109-6delinsCT
NM_001302825.1:c.109-7_109-6delinsCT (GHRL)	NP_001289754.1:n.109-7_109-6delinsCT
NM_016362.4:c.109-7_109-6delinsCT (GHRL)	NP_057446.1:n.109-7_109-6delinsCT
NR_004431.3:n.383+1782_383+1783delinsAG (GHRLOS)
NR_024144.2:n.466+1782_466+1783delinsAG (GHRLOS)
NR_024145.2:n.555+1782_555+1783delinsAG (GHRLOS)
NR_073566.1:n.566+1778_566+1779delinsAG (GHRLOS)
NR_073567.1:n.554+1782_554+1783delinsAG (GHRLOS)
NR_073568.1:n.409+1782_409+1783delinsAG (GHRLOS)
NR_126505.1:n.106+2957_106+2958delinsCT (GHRL)
XM_017006612.2:c.109-7_109-6delinsCT (GHRL)	XP_016862101.1:n.109-7_109-6delinsCT
XM_017006613.2:c.109-10_109-9delinsCT (GHRL)	XP_016862102.1:n.109-10_109-9delinsCT
XM_024453594.1:c.109-7_109-6delinsCT (GHRL)	XP_024309362.1:n.109-7_109-6delinsCT
NM_001134941.3:c.109-10_109-9delinsCT (GHRL)	NP_001128413.1:n.109-10_109-9delinsCT
NM_001134944.2:c.73-7_73-6delinsCT (GHRL)	NP_001128416.1:n.73-7_73-6delinsCT
NM_001134945.2:c.73-10_73-9delinsCT (GHRL)	NP_001128417.1:n.73-10_73-9delinsCT
NM_001134946.2:c.72+2957_72+2958delinsCT (GHRL)	NP_001128418.1:n.72+2957_72+2958delinsCT
NM_001302821.2:c.109-7_109-6delinsCT (GHRL)	NP_001289750.1:n.109-7_109-6delinsCT
NM_001302822.2:c.109-7_109-6delinsCT (GHRL)	NP_001289751.1:n.109-7_109-6delinsCT
NM_001302823.2:c.109-10_109-9delinsCT (GHRL)	NP_001289752.1:n.109-10_109-9delinsCT
NM_001302824.2:c.109-7_109-6delinsCT (GHRL)	NP_001289753.1:n.109-7_109-6delinsCT
NM_001302825.2:c.109-7_109-6delinsCT (GHRL)	NP_001289754.1:n.109-7_109-6delinsCT
NM_016362.5:c.109-7_109-6delinsCT (GHRL) MANE Select	NP_057446.1:n.109-7_109-6delinsCT
NR_126505.2:n.106+2957_106+2958delinsCT (GHRL)