Canonical Allele Identifier: CA1139532952

Gene: GCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54865381del , CM000676.2:g.54865381del	GRCh38
NC_000014.8:g.55332099del , CM000676.1:g.55332099del	GRCh37
NC_000014.7:g.54401849del	NCBI36
NG_008647.1:g.42445del

Transcript Alleles

HGVS	Amino-acid change
ENST00000491895.7:c.400del MANE Select	ENSP00000419045.2:p.Asp134ThrfsTer2
ENST00000254299.8:n.548del
ENST00000395514.5:c.400del	ENSP00000378890.1:p.Asp134ThrfsTer2
ENST00000395521.6:n.183del
ENST00000491895.6:c.400del	ENSP00000419045.2:p.Asp134ThrfsTer2
ENST00000536224.2:c.400del	ENSP00000445246.2:p.Asp134ThrfsTer2
ENST00000543643.6:c.400del	ENSP00000444011.2:p.Asp134ThrfsTer2
ENST00000622544.4:c.400del	ENSP00000477796.1:p.Asp134ThrfsTer2
NM_000161.2:c.400del	NP_000152.1:p.Asp134ThrfsTer2
NM_001024024.1:c.400del	NP_001019195.1:p.Asp134ThrfsTer2
NM_001024070.1:c.400del	NP_001019241.1:p.Asp134ThrfsTer2
NM_001024071.1:c.400del	NP_001019242.1:p.Asp134ThrfsTer2
XM_005267530.1:c.400del	XP_005267587.1:p.Asp134ThrfsTer2
XM_011536643.1:c.400del	XP_011534945.1:p.Asp134ThrfsTer2
XM_017021218.1:c.106del	XP_016876707.1:p.Asp36ThrfsTer2
NM_000161.3:c.400del MANE Select	NP_000152.1:p.Asp134ThrfsTer2
NM_001024070.2:c.400del	NP_001019241.1:p.Asp134ThrfsTer2
NM_001024071.2:c.400del	NP_001019242.1:p.Asp134ThrfsTer2
NM_001024024.2:c.400del	NP_001019195.1:p.Asp134ThrfsTer2