Canonical Allele Identifier: CA614283813

Gene: GCH1

Linked Data

• dbSNP Id: rs1401973688
• gnomAD v2: 14-55310436-A-G
• gnomAD v3: 14-54843718-A-G
• gnomAD v4: 14-54843718-A-G
• MyVariant Identifiers: chr14:g.55310436A>G (hg19) ; chr14:g.54843718A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54843718A>G , CM000676.2:g.54843718A>G	GRCh38
NC_000014.8:g.55310436A>G , CM000676.1:g.55310436A>G	GRCh37
NC_000014.7:g.54380186A>G	NCBI36
NG_008647.1:g.64107T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.*299T>C MANE Select	ENSP00000419045.2:n.*299T>C
ENST00000254299.8:n.1200T>C
ENST00000395514.5:c.*16+283T>C	ENSP00000378890.1:n.*16+283T>C
ENST00000395521.6:n.293-664T>C
ENST00000491895.6:c.*299T>C	ENSP00000419045.2:n.*299T>C
ENST00000536224.2:c.627-664T>C	ENSP00000445246.2:n.627-664T>C
ENST00000543643.6:c.*12+64T>C	ENSP00000444011.2:n.*12+64T>C
ENST00000622544.4:c.*299T>C	ENSP00000477796.1:n.*299T>C
NM_000161.2:c.*299T>C	NP_000152.1:n.*299T>C
NM_001024024.1:c.*16+283T>C	NP_001019195.1:n.*16+283T>C
NM_001024070.1:c.*12+64T>C	NP_001019241.1:n.*12+64T>C
NM_001024071.1:c.627-664T>C	NP_001019242.1:n.627-664T>C
XM_005267530.1:c.*76T>C	XP_005267587.1:n.*76T>C
XM_017021218.1:c.*299T>C	XP_016876707.1:n.*299T>C
NM_000161.3:c.*299T>C MANE Select	NP_000152.1:n.*299T>C
NM_001024070.2:c.*12+64T>C	NP_001019241.1:n.*12+64T>C
NM_001024071.2:c.627-664T>C	NP_001019242.1:n.627-664T>C
NM_001024024.2:c.*16+283T>C	NP_001019195.1:n.*16+283T>C