Canonical Allele Identifier: CA2270149512

Gene: GH1 CSHL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63917975A= , CM000679.2:g.63917975A=	GRCh38
NC_000017.10:g.61995335A= , CM000679.1:g.61995335A=	GRCh37
NC_000017.9:g.59349067A=	NCBI36
NG_011676.1:g.5864T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323322.10:c.291+42T= (GH1) MANE Select	ENSP00000312673.5:n.291+42T=
ENST00000647774.1:c.569+42T=
ENST00000323322.9:c.291+42T= (GH1)	ENSP00000312673.5:n.291+42T=
ENST00000342364.8:c.171+371T= (GH1)	ENSP00000339278.4:n.171+371T=
ENST00000351388.8:c.172-51T= (GH1)	ENSP00000343791.4:n.172-51T=
ENST00000392824.8:c.10+792T= (CSHL1)	ENSP00000376569.5:n.10+792T=
ENST00000458650.6:c.246+42T= (GH1)	ENSP00000408486.2:n.246+42T=
ENST00000579711.1:n.652+42T= (GH1)
ENST00000617086.1:c.11-469T= (GH1)	ENSP00000481276.1:n.11-469T=
NM_000515.4:c.291+42T= (GH1)	NP_000506.2:n.291+42T=
NM_022559.3:c.246+42T= (GH1)	NP_072053.1:n.246+42T=
NM_022560.3:c.172-51T= (GH1)	NP_072054.1:n.172-51T=
XM_011524612.1:c.291+42T= (GH1)	XP_011522914.1:n.291+42T=
NM_000515.5:c.291+42T= (GH1) MANE Select	NP_000506.2:n.291+42T=
NM_022559.4:c.246+42T= (GH1)	NP_072053.1:n.246+42T=
NM_022560.4:c.172-51T= (GH1)	NP_072054.1:n.172-51T=