Canonical Allele Identifier: CA2801650434

Gene: GCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54843675C>A , CM000676.2:g.54843675C>A	GRCh38
NC_000014.8:g.55310393C>A , CM000676.1:g.55310393C>A	GRCh37
NC_000014.7:g.54380143C>A	NCBI36
NG_008647.1:g.64150G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.*342G>T MANE Select	ENSP00000419045.2:n.*342G>T
ENST00000254299.8:n.1243G>T
ENST00000395514.5:c.*16+326G>T	ENSP00000378890.1:n.*16+326G>T
ENST00000395521.6:n.293-621G>T
ENST00000491895.6:c.*342G>T	ENSP00000419045.2:n.*342G>T
ENST00000536224.2:c.627-621G>T	ENSP00000445246.2:n.627-621G>T
ENST00000543643.6:c.*12+107G>T	ENSP00000444011.2:n.*12+107G>T
ENST00000622544.4:c.*342G>T	ENSP00000477796.1:n.*342G>T
NM_000161.2:c.*342G>T	NP_000152.1:n.*342G>T
NM_001024024.1:c.*16+326G>T	NP_001019195.1:n.*16+326G>T
NM_001024070.1:c.*12+107G>T	NP_001019241.1:n.*12+107G>T
NM_001024071.1:c.627-621G>T	NP_001019242.1:n.627-621G>T
XM_005267530.1:c.*119G>T	XP_005267587.1:n.*119G>T
XM_017021218.1:c.*342G>T	XP_016876707.1:n.*342G>T
NM_000161.3:c.*342G>T MANE Select	NP_000152.1:n.*342G>T
NM_001024070.2:c.*12+107G>T	NP_001019241.1:n.*12+107G>T
NM_001024071.2:c.627-621G>T	NP_001019242.1:n.627-621G>T
NM_001024024.2:c.*16+326G>T	NP_001019195.1:n.*16+326G>T