Canonical Allele Identifier: CA706904703

Gene: GCH1

Linked Data

• dbSNP Id: rs1304099248
• MyVariant Identifiers: chr14:g.55311467C>T (hg19) ; chr14:g.54844749C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54844749C>T , CM000676.2:g.54844749C>T	GRCh38
NC_000014.8:g.55311467C>T , CM000676.1:g.55311467C>T	GRCh37
NC_000014.7:g.54381217C>T	NCBI36
NG_008647.1:g.63076G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.627-606G>A MANE Select	ENSP00000419045.2:n.627-606G>A
ENST00000254299.8:n.775-606G>A
ENST00000395514.5:c.627-606G>A	ENSP00000378890.1:n.627-606G>A
ENST00000395521.6:n.293-1695G>A
ENST00000491895.6:c.627-606G>A	ENSP00000419045.2:n.627-606G>A
ENST00000536224.2:c.626+1019G>A	ENSP00000445246.2:n.626+1019G>A
ENST00000543643.6:c.627-880G>A	ENSP00000444011.2:n.627-880G>A
ENST00000622544.4:c.627-606G>A	ENSP00000477796.1:n.627-606G>A
NM_000161.2:c.627-606G>A	NP_000152.1:n.627-606G>A
NM_001024024.1:c.627-606G>A	NP_001019195.1:n.627-606G>A
NM_001024070.1:c.627-880G>A	NP_001019241.1:n.627-880G>A
NM_001024071.1:c.626+1019G>A	NP_001019242.1:n.626+1019G>A
XM_005267530.1:c.627-880G>A	XP_005267587.1:n.627-880G>A
XM_017021218.1:c.333-606G>A	XP_016876707.1:n.333-606G>A
NM_000161.3:c.627-606G>A MANE Select	NP_000152.1:n.627-606G>A
NM_001024070.2:c.627-880G>A	NP_001019241.1:n.627-880G>A
NM_001024071.2:c.626+1019G>A	NP_001019242.1:n.626+1019G>A
NM_001024024.2:c.627-606G>A	NP_001019195.1:n.627-606G>A