Canonical Allele Identifier: CA2639307309

Gene: GH1 CSHL1

Linked Data

• gnomAD v4: 17-63917739-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63917740del , CM000679.2:g.63917740del	GRCh38
NC_000017.10:g.61995100del , CM000679.1:g.61995100del	GRCh37
NC_000017.9:g.59348832del	NCBI36
NG_011676.1:g.6099del

Transcript Alleles

HGVS	Amino-acid change
ENST00000323322.10:c.456+20del (GH1) MANE Select	ENSP00000312673.5:n.456+20del
ENST00000647774.1:c.734+20del
ENST00000323322.9:c.456+20del (GH1)	ENSP00000312673.5:n.456+20del
ENST00000342364.8:c.172-234del (GH1)	ENSP00000339278.4:n.172-234del
ENST00000351388.8:c.336+20del (GH1)	ENSP00000343791.4:n.336+20del
ENST00000392824.8:c.10+1027del (CSHL1)	ENSP00000376569.5:n.10+1027del
ENST00000458650.6:c.411+20del (GH1)	ENSP00000408486.2:n.411+20del
ENST00000579711.1:n.817+20del (GH1)
ENST00000617086.1:c.11-234del (GH1)	ENSP00000481276.1:n.11-234del
NM_000515.4:c.456+20del (GH1)	NP_000506.2:n.456+20del
NM_022559.3:c.411+20del (GH1)	NP_072053.1:n.411+20del
NM_022560.3:c.336+20del (GH1)	NP_072054.1:n.336+20del
XM_011524612.1:c.456+20del (GH1)	XP_011522914.1:n.456+20del
XR_002958148.1:n.389-50del
NM_000515.5:c.456+20del (GH1) MANE Select	NP_000506.2:n.456+20del
NM_022559.4:c.411+20del (GH1)	NP_072053.1:n.411+20del
NM_022560.4:c.336+20del (GH1)	NP_072054.1:n.336+20del