Canonical Allele Identifier: CA2577505985

Gene: GHRL GHRLOS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10289830_10289833del , CM000665.2:g.10289830_10289833del	GRCh38
NC_000003.11:g.10331514_10331517del , CM000665.1:g.10331514_10331517del	GRCh37
NC_000003.10:g.10306514_10306517del	NCBI36
NG_011560.1:g.8115_8118del
NG_033090.1:g.13879_13882del
NG_033090.2:g.13879_13882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335542.13:c.154_157del (GHRL) MANE Select	ENSP00000335074.8:p.Ala52Ter
ENST00000287656.11:c.151_154del (GHRL)	ENSP00000287656.7:p.Ala51Ter
ENST00000335542.12:c.154_157del (GHRL)	ENSP00000335074.8:p.Ala52Ter
ENST00000422159.5:c.154_157del (GHRL)	ENSP00000405464.1:p.Ala52Ter
ENST00000429122.1:c.154_157del (GHRL)	ENSP00000414819.1:p.Ala52Ter
ENST00000430179.5:c.151_154del (GHRL)	ENSP00000399922.1:p.Ala51Ter
ENST00000437422.6:c.118_121del (GHRL)	ENSP00000416768.2:p.Ala40Ter
ENST00000439975.6:c.72+3009_72+3012del (GHRL)	ENSP00000403725.2:n.72+3009_72+3012del
ENST00000446937.2:c.72+3009_72+3012del (GHRL)	ENSP00000394923.2:n.72+3009_72+3012del
ENST00000449238.6:c.115_118del (GHRL)	ENSP00000388145.2:p.Ala39Ter
ENST00000457360.5:c.154_157del (GHRL)	ENSP00000391406.1:p.Ala52Ter
ENST00000481287.5:n.331_334del (GHRL)
ENST00000491589.5:n.245_248del (GHRL)
NM_001134941.2:c.151_154del (GHRL)	NP_001128413.1:p.Ala51Ter
NM_001134944.1:c.118_121del (GHRL)	NP_001128416.1:p.Ala40Ter
NM_001134945.1:c.115_118del (GHRL)	NP_001128417.1:p.Ala39Ter
NM_001134946.1:c.72+3009_72+3012del (GHRL)	NP_001128418.1:n.72+3009_72+3012del
NM_001302821.1:c.154_157del (GHRL)	NP_001289750.1:p.Ala52Ter
NM_001302822.1:c.154_157del (GHRL)	NP_001289751.1:p.Ala52Ter
NM_001302823.1:c.151_154del (GHRL)	NP_001289752.1:p.Ala51Ter
NM_001302824.1:c.154_157del (GHRL)	NP_001289753.1:p.Ala52Ter
NM_001302825.1:c.154_157del (GHRL)	NP_001289754.1:p.Ala52Ter
NM_016362.4:c.154_157del (GHRL)	NP_057446.1:p.Ala52Ter
NR_004431.3:n.383+1728_383+1731del (GHRLOS)
NR_024144.2:n.466+1728_466+1731del (GHRLOS)
NR_024145.2:n.555+1728_555+1731del (GHRLOS)
NR_073566.1:n.566+1724_566+1727del (GHRLOS)
NR_073567.1:n.554+1728_554+1731del (GHRLOS)
NR_073568.1:n.409+1728_409+1731del (GHRLOS)
NR_126505.1:n.106+3009_106+3012del (GHRL)
XM_017006612.2:c.154_157del (GHRL)	XP_016862101.1:p.Ala52Ter
XM_017006613.2:c.151_154del (GHRL)	XP_016862102.1:p.Ala51Ter
XM_024453594.1:c.154_157del (GHRL)	XP_024309362.1:p.Ala52Ter
NM_001134941.3:c.151_154del (GHRL)	NP_001128413.1:p.Ala51Ter
NM_001134944.2:c.118_121del (GHRL)	NP_001128416.1:p.Ala40Ter
NM_001134945.2:c.115_118del (GHRL)	NP_001128417.1:p.Ala39Ter
NM_001134946.2:c.72+3009_72+3012del (GHRL)	NP_001128418.1:n.72+3009_72+3012del
NM_001302821.2:c.154_157del (GHRL)	NP_001289750.1:p.Ala52Ter
NM_001302822.2:c.154_157del (GHRL)	NP_001289751.1:p.Ala52Ter
NM_001302823.2:c.151_154del (GHRL)	NP_001289752.1:p.Ala51Ter
NM_001302824.2:c.154_157del (GHRL)	NP_001289753.1:p.Ala52Ter
NM_001302825.2:c.154_157del (GHRL)	NP_001289754.1:p.Ala52Ter
NM_016362.5:c.154_157del (GHRL) MANE Select	NP_057446.1:p.Ala52Ter
NR_126505.2:n.106+3009_106+3012del (GHRL)