Canonical Allele Identifier: CA400612088

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63917903A>G , CM000679.2:g.63917903A>G GRCh38
NC_000017.10:g.61995263A>G , CM000679.1:g.61995263A>G GRCh37
NC_000017.9:g.59348995A>G NCBI36
NG_011676.1:g.5936T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323322.10:c.313T>C (GH1) MANE Select ENSP00000312673.5:p.Ser105Pro
ENST00000647774.1:c.591T>C
ENST00000323322.9:c.313T>C (GH1) ENSP00000312673.5:p.Ser105Pro
ENST00000342364.8:c.172-397T>C (GH1) ENSP00000339278.4:n.172-397T>C
ENST00000351388.8:c.193T>C (GH1) ENSP00000343791.4:p.Ser65Pro
ENST00000392824.8:c.10+864T>C (CSHL1) ENSP00000376569.5:n.10+864T>C
ENST00000458650.6:c.268T>C (GH1) ENSP00000408486.2:p.Ser90Pro
ENST00000579711.1:n.674T>C (GH1)
ENST00000617086.1:c.11-397T>C (GH1) ENSP00000481276.1:n.11-397T>C
NM_000515.4:c.313T>C (GH1) NP_000506.2:p.Ser105Pro
NM_022559.3:c.268T>C (GH1) NP_072053.1:p.Ser90Pro
NM_022560.3:c.193T>C (GH1) NP_072054.1:p.Ser65Pro
XM_011524612.1:c.313T>C (GH1) XP_011522914.1:p.Ser105Pro
NM_000515.5:c.313T>C (GH1) MANE Select NP_000506.2:p.Ser105Pro
NM_022559.4:c.268T>C (GH1) NP_072053.1:p.Ser90Pro
NM_022560.4:c.193T>C (GH1) NP_072054.1:p.Ser65Pro