Canonical Allele Identifier: CA2138218000

Gene: GCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54843618T= , CM000676.2:g.54843618T=	GRCh38
NC_000014.8:g.55310336T= , CM000676.1:g.55310336T=	GRCh37
NC_000014.7:g.54380086T=	NCBI36
NG_008647.1:g.64207A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.*399A= MANE Select	ENSP00000419045.2:n.*399A=
ENST00000254299.8:n.1300A=
ENST00000395514.5:c.*16+383A=	ENSP00000378890.1:n.*16+383A=
ENST00000395521.6:n.293-564A=
ENST00000491895.6:c.*399A=	ENSP00000419045.2:n.*399A=
ENST00000536224.2:c.627-564A=	ENSP00000445246.2:n.627-564A=
ENST00000543643.6:c.*12+164A=	ENSP00000444011.2:n.*12+164A=
ENST00000622544.4:c.*399A=	ENSP00000477796.1:n.*399A=
NM_000161.2:c.*399A=	NP_000152.1:n.*399A=
NM_001024024.1:c.*16+383A=	NP_001019195.1:n.*16+383A=
NM_001024070.1:c.*12+164A=	NP_001019241.1:n.*12+164A=
NM_001024071.1:c.627-564A=	NP_001019242.1:n.627-564A=
XM_005267530.1:c.*176A=	XP_005267587.1:n.*176A=
XM_017021218.1:c.*399A=	XP_016876707.1:n.*399A=
NM_000161.3:c.*399A= MANE Select	NP_000152.1:n.*399A=
NM_001024070.2:c.*12+164A=	NP_001019241.1:n.*12+164A=
NM_001024071.2:c.627-564A=	NP_001019242.1:n.627-564A=
NM_001024024.2:c.*16+383A=	NP_001019195.1:n.*16+383A=