Canonical Allele Identifier: CA2639307305

Gene: GH1 CSHL1

Linked Data

• gnomAD v4: 17-63917733-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63917735del , CM000679.2:g.63917735del	GRCh38
NC_000017.10:g.61995095del , CM000679.1:g.61995095del	GRCh37
NC_000017.9:g.59348827del	NCBI36
NG_011676.1:g.6105del

Transcript Alleles

HGVS	Amino-acid change
ENST00000323322.10:c.456+26del (GH1) MANE Select	ENSP00000312673.5:n.456+26del
ENST00000647774.1:c.734+26del
ENST00000323322.9:c.456+26del (GH1)	ENSP00000312673.5:n.456+26del
ENST00000342364.8:c.172-228del (GH1)	ENSP00000339278.4:n.172-228del
ENST00000351388.8:c.336+26del (GH1)	ENSP00000343791.4:n.336+26del
ENST00000392824.8:c.10+1033del (CSHL1)	ENSP00000376569.5:n.10+1033del
ENST00000458650.6:c.411+26del (GH1)	ENSP00000408486.2:n.411+26del
ENST00000579711.1:n.817+26del (GH1)
ENST00000617086.1:c.11-228del (GH1)	ENSP00000481276.1:n.11-228del
NM_000515.4:c.456+26del (GH1)	NP_000506.2:n.456+26del
NM_022559.3:c.411+26del (GH1)	NP_072053.1:n.411+26del
NM_022560.3:c.336+26del (GH1)	NP_072054.1:n.336+26del
XM_011524612.1:c.456+26del (GH1)	XP_011522914.1:n.456+26del
XR_002958148.1:n.389-55del
NM_000515.5:c.456+26del (GH1) MANE Select	NP_000506.2:n.456+26del
NM_022559.4:c.411+26del (GH1)	NP_072053.1:n.411+26del
NM_022560.4:c.336+26del (GH1)	NP_072054.1:n.336+26del