Canonical Allele Identifier: CA389790125

Gene: GCH1

Linked Data

• ClinVar Variation Id: 431944
• ClinVar RCV Id: RCV001857005
• dbSNP Id: rs1555360034
• MyVariant Identifiers: chr14:g.55332103A>G (hg19) ; chr14:g.54865385A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54865385A>G , CM000676.2:g.54865385A>G	GRCh38
NC_000014.8:g.55332103A>G , CM000676.1:g.55332103A>G	GRCh37
NC_000014.7:g.54401853A>G	NCBI36
NG_008647.1:g.42440T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000491895.7:c.395T>C MANE Select	ENSP00000419045.2:p.Val132Ala
ENST00000254299.8:n.543T>C
ENST00000395514.5:c.395T>C	ENSP00000378890.1:p.Val132Ala
ENST00000395521.6:n.178T>C
ENST00000491895.6:c.395T>C	ENSP00000419045.2:p.Val132Ala
ENST00000536224.2:c.395T>C	ENSP00000445246.2:p.Val132Ala
ENST00000543643.6:c.395T>C	ENSP00000444011.2:p.Val132Ala
ENST00000622544.4:c.395T>C	ENSP00000477796.1:p.Val132Ala
NM_000161.2:c.395T>C	NP_000152.1:p.Val132Ala
NM_001024024.1:c.395T>C	NP_001019195.1:p.Val132Ala
NM_001024070.1:c.395T>C	NP_001019241.1:p.Val132Ala
NM_001024071.1:c.395T>C	NP_001019242.1:p.Val132Ala
XM_005267530.1:c.395T>C	XP_005267587.1:p.Val132Ala
XM_011536643.1:c.395T>C	XP_011534945.1:p.Val132Ala
XM_017021218.1:c.101T>C	XP_016876707.1:p.Val34Ala
NM_000161.3:c.395T>C MANE Select	NP_000152.1:p.Val132Ala
NM_001024070.2:c.395T>C	NP_001019241.1:p.Val132Ala
NM_001024071.2:c.395T>C	NP_001019242.1:p.Val132Ala
NM_001024024.2:c.395T>C	NP_001019195.1:p.Val132Ala