Canonical Allele Identifier: CA260542090

Gene: GCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54842959C>T , CM000676.2:g.54842959C>T	GRCh38
NC_000014.8:g.55309677C>T , CM000676.1:g.55309677C>T	GRCh37
NC_000014.7:g.54379427C>T	NCBI36
NG_008647.1:g.64866G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.*1058G>A MANE Select	ENSP00000419045.2:n.*1058G>A
ENST00000254299.8:n.1959G>A
ENST00000395514.5:c.*112G>A	ENSP00000378890.1:n.*112G>A
ENST00000491895.6:c.*1058G>A	ENSP00000419045.2:n.*1058G>A
ENST00000536224.2:c.*80G>A	ENSP00000445246.2:n.*80G>A
ENST00000543643.6:c.*108G>A	ENSP00000444011.2:n.*108G>A
ENST00000622544.4:c.*1058G>A	ENSP00000477796.1:n.*1058G>A
NM_000161.2:c.*1058G>A	NP_000152.1:n.*1058G>A
NM_001024024.1:c.*112G>A	NP_001019195.1:n.*112G>A
NM_001024070.1:c.*108G>A	NP_001019241.1:n.*108G>A
NM_001024071.1:c.*80G>A	NP_001019242.1:n.*80G>A
XM_005267530.1:c.*835G>A	XP_005267587.1:n.*835G>A
XM_017021218.1:c.*1058G>A	XP_016876707.1:n.*1058G>A
NM_000161.3:c.*1058G>A MANE Select	NP_000152.1:n.*1058G>A
NM_001024070.2:c.*108G>A	NP_001019241.1:n.*108G>A
NM_001024071.2:c.*80G>A	NP_001019242.1:n.*80G>A
NM_001024024.2:c.*112G>A	NP_001019195.1:n.*112G>A