Canonical Allele Identifier: CA2138218992

Gene: GCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54845851A= , CM000676.2:g.54845851A=	GRCh38
NC_000014.8:g.55312569A= , CM000676.1:g.55312569A=	GRCh37
NC_000014.7:g.54382319A=	NCBI36
NG_008647.1:g.61974T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.543T= MANE Select	ENSP00000419045.2:p.Val181=
ENST00000254299.8:n.691T=
ENST00000395514.5:c.543T=	ENSP00000378890.1:p.Val181=
ENST00000395521.6:n.293-2797T=
ENST00000491895.6:c.543T=	ENSP00000419045.2:p.Val181=
ENST00000536224.2:c.543T=	ENSP00000445246.2:p.Val181=
ENST00000543643.6:c.543T=	ENSP00000444011.2:p.Val181=
ENST00000622544.4:c.543T=	ENSP00000477796.1:p.Val181=
NM_000161.2:c.543T=	NP_000152.1:p.Val181=
NM_001024024.1:c.543T=	NP_001019195.1:p.Val181=
NM_001024070.1:c.543T=	NP_001019241.1:p.Val181=
NM_001024071.1:c.543T=	NP_001019242.1:p.Val181=
XM_005267530.1:c.543T=	XP_005267587.1:p.Val181=
XM_017021218.1:c.249T=	XP_016876707.1:p.Val83=
NM_000161.3:c.543T= MANE Select	NP_000152.1:p.Val181=
NM_001024070.2:c.543T=	NP_001019241.1:p.Val181=
NM_001024071.2:c.543T=	NP_001019242.1:p.Val181=
NM_001024024.2:c.543T=	NP_001019195.1:p.Val181=