Canonical Allele Identifier: CA351779002

Gene: GHRL GHRLOS

Linked Data

• MyVariant Identifiers: chr3:g.10331502G>C (hg19) ; chr3:g.10289818G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10289818G>C , CM000665.2:g.10289818G>C	GRCh38
NC_000003.11:g.10331502G>C , CM000665.1:g.10331502G>C	GRCh37
NC_000003.10:g.10306502G>C	NCBI36
NG_011560.1:g.8130C>G
NG_033090.1:g.13867G>C
NG_033090.2:g.13867G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335542.13:c.169C>G (GHRL) MANE Select	ENSP00000335074.8:p.Leu57Val
ENST00000287656.11:c.166C>G (GHRL)	ENSP00000287656.7:p.Leu56Val
ENST00000335542.12:c.169C>G (GHRL)	ENSP00000335074.8:p.Leu57Val
ENST00000422159.5:c.169C>G (GHRL)	ENSP00000405464.1:p.Leu57Val
ENST00000429122.1:c.169C>G (GHRL)	ENSP00000414819.1:p.Leu57Val
ENST00000430179.5:c.166C>G (GHRL)	ENSP00000399922.1:p.Leu56Val
ENST00000437422.6:c.133C>G (GHRL)	ENSP00000416768.2:p.Leu45Val
ENST00000439975.6:c.73-3006C>G (GHRL)	ENSP00000403725.2:n.73-3006C>G
ENST00000446937.2:c.72+3024C>G (GHRL)	ENSP00000394923.2:n.72+3024C>G
ENST00000449238.6:c.130C>G (GHRL)	ENSP00000388145.2:p.Leu44Val
ENST00000457360.5:c.169C>G (GHRL)	ENSP00000391406.1:p.Leu57Val
ENST00000481287.5:n.346C>G (GHRL)
ENST00000491589.5:n.260C>G (GHRL)
NM_001134941.2:c.166C>G (GHRL)	NP_001128413.1:p.Leu56Val
NM_001134944.1:c.133C>G (GHRL)	NP_001128416.1:p.Leu45Val
NM_001134945.1:c.130C>G (GHRL)	NP_001128417.1:p.Leu44Val
NM_001134946.1:c.73-3006C>G (GHRL)	NP_001128418.1:n.73-3006C>G
NM_001302821.1:c.169C>G (GHRL)	NP_001289750.1:p.Leu57Val
NM_001302822.1:c.169C>G (GHRL)	NP_001289751.1:p.Leu57Val
NM_001302823.1:c.166C>G (GHRL)	NP_001289752.1:p.Leu56Val
NM_001302824.1:c.169C>G (GHRL)	NP_001289753.1:p.Leu57Val
NM_001302825.1:c.169C>G (GHRL)	NP_001289754.1:p.Leu57Val
NM_016362.4:c.169C>G (GHRL)	NP_057446.1:p.Leu57Val
NR_004431.3:n.383+1716G>C (GHRLOS)
NR_024144.2:n.466+1716G>C (GHRLOS)
NR_024145.2:n.555+1716G>C (GHRLOS)
NR_073566.1:n.566+1712G>C (GHRLOS)
NR_073567.1:n.554+1716G>C (GHRLOS)
NR_073568.1:n.409+1716G>C (GHRLOS)
NR_126505.1:n.106+3024C>G (GHRL)
XM_017006612.2:c.169C>G (GHRL)	XP_016862101.1:p.Leu57Val
XM_017006613.2:c.166C>G (GHRL)	XP_016862102.1:p.Leu56Val
XM_024453594.1:c.169C>G (GHRL)	XP_024309362.1:p.Leu57Val
NM_001134941.3:c.166C>G (GHRL)	NP_001128413.1:p.Leu56Val
NM_001134944.2:c.133C>G (GHRL)	NP_001128416.1:p.Leu45Val
NM_001134945.2:c.130C>G (GHRL)	NP_001128417.1:p.Leu44Val
NM_001134946.2:c.73-3006C>G (GHRL)	NP_001128418.1:n.73-3006C>G
NM_001302821.2:c.169C>G (GHRL)	NP_001289750.1:p.Leu57Val
NM_001302822.2:c.169C>G (GHRL)	NP_001289751.1:p.Leu57Val
NM_001302823.2:c.166C>G (GHRL)	NP_001289752.1:p.Leu56Val
NM_001302824.2:c.169C>G (GHRL)	NP_001289753.1:p.Leu57Val
NM_001302825.2:c.169C>G (GHRL)	NP_001289754.1:p.Leu57Val
NM_016362.5:c.169C>G (GHRL) MANE Select	NP_057446.1:p.Leu57Val
NR_126505.2:n.106+3024C>G (GHRL)