Canonical Allele Identifier: CA2499222644

Gene: GCH1

Linked Data

• ClinVar Variation Id: 1298582
• ClinVar RCV Id: RCV001726912
• dbSNP Id: rs2140127251

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54902441_54902444dup , CM000676.2:g.54902441_54902444dup	GRCh38
NC_000014.8:g.55369159_55369162dup , CM000676.1:g.55369159_55369162dup	GRCh37
NC_000014.7:g.54438909_54438912dup	NCBI36
NG_008647.1:g.5381_5384dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000491895.7:c.220_223dup MANE Select	ENSP00000419045.2:p.Tyr75CysfsTer?
ENST00000254299.8:n.368_371dup
ENST00000395514.5:c.220_223dup	ENSP00000378890.1:p.Tyr75CysfsTer?
ENST00000395521.6:n.3_6dup
ENST00000491895.6:c.220_223dup	ENSP00000419045.2:p.Tyr75CysfsTer?
ENST00000536224.2:c.220_223dup	ENSP00000445246.2:p.Tyr75CysfsTer?
ENST00000543643.6:c.220_223dup	ENSP00000444011.2:p.Tyr75CysfsTer?
ENST00000622544.4:c.220_223dup	ENSP00000477796.1:p.Tyr75CysfsTer?
NM_000161.2:c.220_223dup	NP_000152.1:p.Tyr75CysfsTer?
NM_001024024.1:c.220_223dup	NP_001019195.1:p.Tyr75CysfsTer?
NM_001024070.1:c.220_223dup	NP_001019241.1:p.Tyr75CysfsTer?
NM_001024071.1:c.220_223dup	NP_001019242.1:p.Tyr75CysfsTer?
XM_005267530.1:c.220_223dup	XP_005267587.1:p.Tyr75CysfsTer?
XM_011536643.1:c.220_223dup	XP_011534945.1:p.Tyr75CysfsTer?
NM_000161.3:c.220_223dup MANE Select	NP_000152.1:p.Tyr75CysfsTer?
NM_001024070.2:c.220_223dup	NP_001019241.1:p.Tyr75CysfsTer?
NM_001024071.2:c.220_223dup	NP_001019242.1:p.Tyr75CysfsTer?
NM_001024024.2:c.220_223dup	NP_001019195.1:p.Tyr75CysfsTer?