Canonical Allele Identifier: CA2270149412

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63917811G= , CM000679.2:g.63917811G= GRCh38
NC_000017.10:g.61995171G= , CM000679.1:g.61995171G= GRCh37
NC_000017.9:g.59348903G= NCBI36
NG_011676.1:g.6028C=

Transcript Alleles

HGVS Amino-acid change
ENST00000323322.10:c.405C= (GH1) MANE Select ENSP00000312673.5:p.Asn135=
ENST00000647774.1:c.683C=
ENST00000323322.9:c.405C= (GH1) ENSP00000312673.5:p.Asn135=
ENST00000342364.8:c.172-305C= (GH1) ENSP00000339278.4:n.172-305C=
ENST00000351388.8:c.285C= (GH1) ENSP00000343791.4:p.Asn95=
ENST00000392824.8:c.10+956C= (CSHL1) ENSP00000376569.5:n.10+956C=
ENST00000458650.6:c.360C= (GH1) ENSP00000408486.2:p.Asn120=
ENST00000579711.1:n.766C= (GH1)
ENST00000617086.1:c.11-305C= (GH1) ENSP00000481276.1:n.11-305C=
NM_000515.4:c.405C= (GH1) NP_000506.2:p.Asn135=
NM_022559.3:c.360C= (GH1) NP_072053.1:p.Asn120=
NM_022560.3:c.285C= (GH1) NP_072054.1:p.Asn95=
XM_011524612.1:c.405C= (GH1) XP_011522914.1:p.Asn135=
XR_002958148.1:n.410G=
NM_000515.5:c.405C= (GH1) MANE Select NP_000506.2:p.Asn135=
NM_022559.4:c.360C= (GH1) NP_072053.1:p.Asn120=
NM_022560.4:c.285C= (GH1) NP_072054.1:p.Asn95=