Canonical Allele Identifier: CA2138251496
Gene: GCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54902415G= , CM000676.2:g.54902415G= GRCh38
NC_000014.8:g.55369133G= , CM000676.1:g.55369133G= GRCh37
NC_000014.7:g.54438883G= NCBI36
NG_008647.1:g.5410C=

Transcript Alleles

HGVS Amino-acid change
ENST00000491895.7:c.249C= MANE Select ENSP00000419045.2:p.Gly83=
ENST00000254299.8:n.397C=
ENST00000395514.5:c.249C= ENSP00000378890.1:p.Gly83=
ENST00000395521.6:n.32C=
ENST00000491895.6:c.249C= ENSP00000419045.2:p.Gly83=
ENST00000536224.2:c.249C= ENSP00000445246.2:p.Gly83=
ENST00000543643.6:c.249C= ENSP00000444011.2:p.Gly83=
ENST00000622544.4:c.249C= ENSP00000477796.1:p.Gly83=
NM_000161.2:c.249C= NP_000152.1:p.Gly83=
NM_001024024.1:c.249C= NP_001019195.1:p.Gly83=
NM_001024070.1:c.249C= NP_001019241.1:p.Gly83=
NM_001024071.1:c.249C= NP_001019242.1:p.Gly83=
XM_005267530.1:c.249C= XP_005267587.1:p.Gly83=
XM_011536643.1:c.249C= XP_011534945.1:p.Gly83=
NM_000161.3:c.249C= MANE Select NP_000152.1:p.Gly83=
NM_001024070.2:c.249C= NP_001019241.1:p.Gly83=
NM_001024071.2:c.249C= NP_001019242.1:p.Gly83=
NM_001024024.2:c.249C= NP_001019195.1:p.Gly83=