Canonical Allele Identifier: CA2138236658
Gene: GCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54882155C= , CM000676.2:g.54882155C= GRCh38
NC_000014.8:g.55348873C= , CM000676.1:g.55348873C= GRCh37
NC_000014.7:g.54418623C= NCBI36
NG_008647.1:g.25670G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000491895.7:c.344-16719G= MANE Select ENSP00000419045.2:n.344-16719G=
ENST00000254299.8:n.492-16719G=
ENST00000395514.5:c.344-16719G= ENSP00000378890.1:n.344-16719G=
ENST00000395521.6:n.127-16719G=
ENST00000491895.6:c.344-16719G= ENSP00000419045.2:n.344-16719G=
ENST00000536224.2:c.344-16719G= ENSP00000445246.2:n.344-16719G=
ENST00000543643.6:c.344-16719G= ENSP00000444011.2:n.344-16719G=
ENST00000622544.4:c.344-16719G= ENSP00000477796.1:n.344-16719G=
NM_000161.2:c.344-16719G= NP_000152.1:n.344-16719G=
NM_001024024.1:c.344-16719G= NP_001019195.1:n.344-16719G=
NM_001024070.1:c.344-16719G= NP_001019241.1:n.344-16719G=
NM_001024071.1:c.344-16719G= NP_001019242.1:n.344-16719G=
XM_005267530.1:c.344-16719G= XP_005267587.1:n.344-16719G=
XM_011536643.1:c.344-16719G= XP_011534945.1:n.344-16719G=
XM_017021218.1:c.-565G= XP_016876707.1:n.-565G=
NM_000161.3:c.344-16719G= MANE Select NP_000152.1:n.344-16719G=
NM_001024070.2:c.344-16719G= NP_001019241.1:n.344-16719G=
NM_001024071.2:c.344-16719G= NP_001019242.1:n.344-16719G=
NM_001024024.2:c.344-16719G= NP_001019195.1:n.344-16719G=