Canonical Allele Identifier: CA389787233

Gene: GCH1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54844137C>G , CM000676.2:g.54844137C>G	GRCh38
NC_000014.8:g.55310855C>G , CM000676.1:g.55310855C>G	GRCh37
NC_000014.7:g.54380605C>G	NCBI36
NG_008647.1:g.63688G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.633G>C MANE Select	ENSP00000419045.2:p.Met211Ile
ENST00000254299.8:n.781G>C
ENST00000395514.5:c.633G>C	ENSP00000378890.1:p.Met211Ile
ENST00000395521.6:n.293-1083G>C
ENST00000491895.6:c.633G>C	ENSP00000419045.2:p.Met211Ile
ENST00000536224.2:c.627-1083G>C	ENSP00000445246.2:n.627-1083G>C
ENST00000543643.6:c.627-268G>C	ENSP00000444011.2:n.627-268G>C
ENST00000622544.4:c.633G>C	ENSP00000477796.1:p.Met211Ile
NM_000161.2:c.633G>C	NP_000152.1:p.Met211Ile
NM_001024024.1:c.633G>C	NP_001019195.1:p.Met211Ile
NM_001024070.1:c.627-268G>C	NP_001019241.1:n.627-268G>C
NM_001024071.1:c.627-1083G>C	NP_001019242.1:n.627-1083G>C
XM_005267530.1:c.627-268G>C	XP_005267587.1:n.627-268G>C
XM_017021218.1:c.339G>C	XP_016876707.1:p.Met113Ile
NM_000161.3:c.633G>C MANE Select	NP_000152.1:p.Met211Ile
NM_001024070.2:c.627-268G>C	NP_001019241.1:n.627-268G>C
NM_001024071.2:c.627-1083G>C	NP_001019242.1:n.627-1083G>C
NM_001024024.2:c.633G>C	NP_001019195.1:p.Met211Ile