Canonical Allele Identifier: CA389786592

Gene: GCH1

Linked Data

• gnomAD v4: 14-54844023-C-A
• MyVariant Identifiers: chr14:g.55310741C>A (hg19) ; chr14:g.54844023C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54844023C>A , CM000676.2:g.54844023C>A	GRCh38
NC_000014.8:g.55310741C>A , CM000676.1:g.55310741C>A	GRCh37
NC_000014.7:g.54380491C>A	NCBI36
NG_008647.1:g.63802G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.747G>T MANE Select	ENSP00000419045.2:p.Arg249Ser
ENST00000254299.8:n.895G>T
ENST00000395514.5:c.747G>T	ENSP00000378890.1:p.Arg249Ser
ENST00000395521.6:n.293-969G>T
ENST00000491895.6:c.747G>T	ENSP00000419045.2:p.Arg249Ser
ENST00000536224.2:c.627-969G>T	ENSP00000445246.2:n.627-969G>T
ENST00000543643.6:c.627-154G>T	ENSP00000444011.2:n.627-154G>T
ENST00000622544.4:c.747G>T	ENSP00000477796.1:p.Arg249Ser
NM_000161.2:c.747G>T	NP_000152.1:p.Arg249Ser
NM_001024024.1:c.747G>T	NP_001019195.1:p.Arg249Ser
NM_001024070.1:c.627-154G>T	NP_001019241.1:n.627-154G>T
NM_001024071.1:c.627-969G>T	NP_001019242.1:n.627-969G>T
XM_005267530.1:c.627-154G>T	XP_005267587.1:n.627-154G>T
XM_017021218.1:c.453G>T	XP_016876707.1:p.Arg151Ser
NM_000161.3:c.747G>T MANE Select	NP_000152.1:p.Arg249Ser
NM_001024070.2:c.627-154G>T	NP_001019241.1:n.627-154G>T
NM_001024071.2:c.627-969G>T	NP_001019242.1:n.627-969G>T
NM_001024024.2:c.747G>T	NP_001019195.1:p.Arg249Ser