Canonical Allele Identifier: CA2138218449
Gene: GCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54844728G= , CM000676.2:g.54844728G= GRCh38
NC_000014.8:g.55311446G= , CM000676.1:g.55311446G= GRCh37
NC_000014.7:g.54381196G= NCBI36
NG_008647.1:g.63097C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000491895.7:c.627-585C= MANE Select ENSP00000419045.2:n.627-585C=
ENST00000254299.8:n.775-585C=
ENST00000395514.5:c.627-585C= ENSP00000378890.1:n.627-585C=
ENST00000395521.6:n.293-1674C=
ENST00000491895.6:c.627-585C= ENSP00000419045.2:n.627-585C=
ENST00000536224.2:c.626+1040C= ENSP00000445246.2:n.626+1040C=
ENST00000543643.6:c.627-859C= ENSP00000444011.2:n.627-859C=
ENST00000622544.4:c.627-585C= ENSP00000477796.1:n.627-585C=
NM_000161.2:c.627-585C= NP_000152.1:n.627-585C=
NM_001024024.1:c.627-585C= NP_001019195.1:n.627-585C=
NM_001024070.1:c.627-859C= NP_001019241.1:n.627-859C=
NM_001024071.1:c.626+1040C= NP_001019242.1:n.626+1040C=
XM_005267530.1:c.627-859C= XP_005267587.1:n.627-859C=
XM_017021218.1:c.333-585C= XP_016876707.1:n.333-585C=
NM_000161.3:c.627-585C= MANE Select NP_000152.1:n.627-585C=
NM_001024070.2:c.627-859C= NP_001019241.1:n.627-859C=
NM_001024071.2:c.626+1040C= NP_001019242.1:n.626+1040C=
NM_001024024.2:c.627-585C= NP_001019195.1:n.627-585C=