Canonical Allele Identifier: CA2695219331
Gene: GCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54902425_54902430del , CM000676.2:g.54902425_54902430del GRCh38
NC_000014.8:g.55369143_55369148del , CM000676.1:g.55369143_55369148del GRCh37
NC_000014.7:g.54438893_54438898del NCBI36
NG_008647.1:g.5396_5401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000491895.7:c.235_240del MANE Select ENSP00000419045.2:p.Leu79_Ser80del
ENST00000254299.8:n.383_388del
ENST00000395514.5:c.235_240del ENSP00000378890.1:p.Leu79_Ser80del
ENST00000395521.6:n.18_23del
ENST00000491895.6:c.235_240del ENSP00000419045.2:p.Leu79_Ser80del
ENST00000536224.2:c.235_240del ENSP00000445246.2:p.Leu79_Ser80del
ENST00000543643.6:c.235_240del ENSP00000444011.2:p.Leu79_Ser80del
ENST00000622544.4:c.235_240del ENSP00000477796.1:p.Leu79_Ser80del
NM_000161.2:c.235_240del NP_000152.1:p.Leu79_Ser80del
NM_001024024.1:c.235_240del NP_001019195.1:p.Leu79_Ser80del
NM_001024070.1:c.235_240del NP_001019241.1:p.Leu79_Ser80del
NM_001024071.1:c.235_240del NP_001019242.1:p.Leu79_Ser80del
XM_005267530.1:c.235_240del XP_005267587.1:p.Leu79_Ser80del
XM_011536643.1:c.235_240del XP_011534945.1:p.Leu79_Ser80del
NM_000161.3:c.235_240del MANE Select NP_000152.1:p.Leu79_Ser80del
NM_001024070.2:c.235_240del NP_001019241.1:p.Leu79_Ser80del
NM_001024071.2:c.235_240del NP_001019242.1:p.Leu79_Ser80del
NM_001024024.2:c.235_240del NP_001019195.1:p.Leu79_Ser80del