Canonical Allele Identifier: CA706930013
Gene: GCH1 HGNC NCBI

Linked Data

dbSNP Id: rs1300303925

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54881130_54881134del , CM000676.2:g.54881130_54881134del GRCh38
NC_000014.8:g.55347848_55347852del , CM000676.1:g.55347848_55347852del GRCh37
NC_000014.7:g.54417598_54417602del NCBI36
NG_008647.1:g.26692_26696del

Transcript Alleles

HGVS Amino-acid Change
ENST00000491895.7:c.344-15697_344-15693del MANE Select ENSP00000419045.2:n.344-15697_344-15693del
ENST00000254299.8:n.492-15697_492-15693del
ENST00000395514.5:c.344-15697_344-15693del ENSP00000378890.1:n.344-15697_344-15693del
ENST00000395521.6:n.127-15697_127-15693del
ENST00000491895.6:c.344-15697_344-15693del ENSP00000419045.2:n.344-15697_344-15693del
ENST00000536224.2:c.344-15697_344-15693del ENSP00000445246.2:n.344-15697_344-15693del
ENST00000543643.6:c.344-15697_344-15693del ENSP00000444011.2:n.344-15697_344-15693del
ENST00000622544.4:c.344-15697_344-15693del ENSP00000477796.1:n.344-15697_344-15693del
NM_000161.2:c.344-15697_344-15693del NP_000152.1:n.344-15697_344-15693del
NM_001024024.1:c.344-15697_344-15693del NP_001019195.1:n.344-15697_344-15693del
NM_001024070.1:c.344-15697_344-15693del NP_001019241.1:n.344-15697_344-15693del
NM_001024071.1:c.344-15697_344-15693del NP_001019242.1:n.344-15697_344-15693del
XM_005267530.1:c.344-15697_344-15693del XP_005267587.1:n.344-15697_344-15693del
XM_011536643.1:c.344-15697_344-15693del XP_011534945.1:n.344-15697_344-15693del
XM_017021218.1:c.49+409_49+413del XP_016876707.1:n.49+409_49+413del
NM_000161.3:c.344-15697_344-15693del MANE Select NP_000152.1:n.344-15697_344-15693del
NM_001024070.2:c.344-15697_344-15693del NP_001019241.1:n.344-15697_344-15693del
NM_001024071.2:c.344-15697_344-15693del NP_001019242.1:n.344-15697_344-15693del
NM_001024024.2:c.344-15697_344-15693del NP_001019195.1:n.344-15697_344-15693del