Canonical Allele Identifier: CA706930180

Gene: GCH1

Linked Data

• dbSNP Id: rs1412088155
• MyVariant Identifiers: chr14:g.55348133G>T (hg19) ; chr14:g.54881415G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54881415G>T , CM000676.2:g.54881415G>T	GRCh38
NC_000014.8:g.55348133G>T , CM000676.1:g.55348133G>T	GRCh37
NC_000014.7:g.54417883G>T	NCBI36
NG_008647.1:g.26410C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000491895.7:c.344-15979C>A MANE Select	ENSP00000419045.2:n.344-15979C>A
ENST00000254299.8:n.492-15979C>A
ENST00000395514.5:c.344-15979C>A	ENSP00000378890.1:n.344-15979C>A
ENST00000395521.6:n.127-15979C>A
ENST00000491895.6:c.344-15979C>A	ENSP00000419045.2:n.344-15979C>A
ENST00000536224.2:c.344-15979C>A	ENSP00000445246.2:n.344-15979C>A
ENST00000543643.6:c.344-15979C>A	ENSP00000444011.2:n.344-15979C>A
ENST00000622544.4:c.344-15979C>A	ENSP00000477796.1:n.344-15979C>A
NM_000161.2:c.344-15979C>A	NP_000152.1:n.344-15979C>A
NM_001024024.1:c.344-15979C>A	NP_001019195.1:n.344-15979C>A
NM_001024070.1:c.344-15979C>A	NP_001019241.1:n.344-15979C>A
NM_001024071.1:c.344-15979C>A	NP_001019242.1:n.344-15979C>A
XM_005267530.1:c.344-15979C>A	XP_005267587.1:n.344-15979C>A
XM_011536643.1:c.344-15979C>A	XP_011534945.1:n.344-15979C>A
XM_017021218.1:c.49+127C>A	XP_016876707.1:n.49+127C>A
NM_000161.3:c.344-15979C>A MANE Select	NP_000152.1:n.344-15979C>A
NM_001024070.2:c.344-15979C>A	NP_001019241.1:n.344-15979C>A
NM_001024071.2:c.344-15979C>A	NP_001019242.1:n.344-15979C>A
NM_001024024.2:c.344-15979C>A	NP_001019195.1:n.344-15979C>A