Canonical Allele Identifier: CA2138217982

Gene: GCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54843574A= , CM000676.2:g.54843574A=	GRCh38
NC_000014.8:g.55310292A= , CM000676.1:g.55310292A=	GRCh37
NC_000014.7:g.54380042A=	NCBI36
NG_008647.1:g.64251T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.*443T= MANE Select	ENSP00000419045.2:n.*443T=
ENST00000254299.8:n.1344T=
ENST00000395514.5:c.*16+427T=	ENSP00000378890.1:n.*16+427T=
ENST00000395521.6:n.293-520T=
ENST00000491895.6:c.*443T=	ENSP00000419045.2:n.*443T=
ENST00000536224.2:c.627-520T=	ENSP00000445246.2:n.627-520T=
ENST00000543643.6:c.*12+208T=	ENSP00000444011.2:n.*12+208T=
ENST00000622544.4:c.*443T=	ENSP00000477796.1:n.*443T=
NM_000161.2:c.*443T=	NP_000152.1:n.*443T=
NM_001024024.1:c.*16+427T=	NP_001019195.1:n.*16+427T=
NM_001024070.1:c.*12+208T=	NP_001019241.1:n.*12+208T=
NM_001024071.1:c.627-520T=	NP_001019242.1:n.627-520T=
XM_005267530.1:c.*220T=	XP_005267587.1:n.*220T=
XM_017021218.1:c.*443T=	XP_016876707.1:n.*443T=
NM_000161.3:c.*443T= MANE Select	NP_000152.1:n.*443T=
NM_001024070.2:c.*12+208T=	NP_001019241.1:n.*12+208T=
NM_001024071.2:c.627-520T=	NP_001019242.1:n.627-520T=
NM_001024024.2:c.*16+427T=	NP_001019195.1:n.*16+427T=