Canonical Allele Identifier: CA2624945024
Gene: GCH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54845862_54845863del , CM000676.2:g.54845862_54845863del GRCh38
NC_000014.8:g.55312580_55312581del , CM000676.1:g.55312580_55312581del GRCh37
NC_000014.7:g.54382330_54382331del NCBI36
NG_008647.1:g.61964_61965del

Transcript Alleles

HGVS Amino-acid Change
ENST00000491895.7:c.542-9_542-8del MANE Select ENSP00000419045.2:n.542-9_542-8del
ENST00000254299.8:n.690-9_690-8del
ENST00000395514.5:c.542-9_542-8del ENSP00000378890.1:n.542-9_542-8del
ENST00000395521.6:n.293-2807_293-2806del
ENST00000491895.6:c.542-9_542-8del ENSP00000419045.2:n.542-9_542-8del
ENST00000536224.2:c.542-9_542-8del ENSP00000445246.2:n.542-9_542-8del
ENST00000543643.6:c.542-9_542-8del ENSP00000444011.2:n.542-9_542-8del
ENST00000622544.4:c.542-9_542-8del ENSP00000477796.1:n.542-9_542-8del
NM_000161.2:c.542-9_542-8del NP_000152.1:n.542-9_542-8del
NM_001024024.1:c.542-9_542-8del NP_001019195.1:n.542-9_542-8del
NM_001024070.1:c.542-9_542-8del NP_001019241.1:n.542-9_542-8del
NM_001024071.1:c.542-9_542-8del NP_001019242.1:n.542-9_542-8del
XM_005267530.1:c.542-9_542-8del XP_005267587.1:n.542-9_542-8del
XM_017021218.1:c.248-9_248-8del XP_016876707.1:n.248-9_248-8del
NM_000161.3:c.542-9_542-8del MANE Select NP_000152.1:n.542-9_542-8del
NM_001024070.2:c.542-9_542-8del NP_001019241.1:n.542-9_542-8del
NM_001024071.2:c.542-9_542-8del NP_001019242.1:n.542-9_542-8del
NM_001024024.2:c.542-9_542-8del NP_001019195.1:n.542-9_542-8del