Canonical Allele Identifier: CA400611713

Gene: GH1 CSHL1

Linked Data

• MyVariant Identifiers: chr17:g.61995181G>T (hg19) ; chr17:g.63917821G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63917821G>T , CM000679.2:g.63917821G>T	GRCh38
NC_000017.10:g.61995181G>T , CM000679.1:g.61995181G>T	GRCh37
NC_000017.9:g.59348913G>T	NCBI36
NG_011676.1:g.6018C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000323322.10:c.395C>A (GH1) MANE Select	ENSP00000312673.5:p.Ser132Tyr
ENST00000647774.1:c.673C>A
ENST00000323322.9:c.395C>A (GH1)	ENSP00000312673.5:p.Ser132Tyr
ENST00000342364.8:c.172-315C>A (GH1)	ENSP00000339278.4:n.172-315C>A
ENST00000351388.8:c.275C>A (GH1)	ENSP00000343791.4:p.Ser92Tyr
ENST00000392824.8:c.10+946C>A (CSHL1)	ENSP00000376569.5:n.10+946C>A
ENST00000458650.6:c.350C>A (GH1)	ENSP00000408486.2:p.Ser117Tyr
ENST00000579711.1:n.756C>A (GH1)
ENST00000617086.1:c.11-315C>A (GH1)	ENSP00000481276.1:n.11-315C>A
NM_000515.4:c.395C>A (GH1)	NP_000506.2:p.Ser132Tyr
NM_022559.3:c.350C>A (GH1)	NP_072053.1:p.Ser117Tyr
NM_022560.3:c.275C>A (GH1)	NP_072054.1:p.Ser92Tyr
XM_011524612.1:c.395C>A (GH1)	XP_011522914.1:p.Ser132Tyr
XR_002958148.1:n.420G>T
NM_000515.5:c.395C>A (GH1) MANE Select	NP_000506.2:p.Ser132Tyr
NM_022559.4:c.350C>A (GH1)	NP_072053.1:p.Ser117Tyr
NM_022560.4:c.275C>A (GH1)	NP_072054.1:p.Ser92Tyr