Canonical Allele Identifier: CA2624944371

Gene: GCH1

Linked Data

• gnomAD v4: 14-54865279-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54865279A>G , CM000676.2:g.54865279A>G	GRCh38
NC_000014.8:g.55331997A>G , CM000676.1:g.55331997A>G	GRCh37
NC_000014.7:g.54401747A>G	NCBI36
NG_008647.1:g.42546T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000491895.7:c.453+48T>C MANE Select	ENSP00000419045.2:n.453+48T>C
ENST00000254299.8:n.601+48T>C
ENST00000395514.5:c.453+48T>C	ENSP00000378890.1:n.453+48T>C
ENST00000395521.6:n.236+48T>C
ENST00000491895.6:c.453+48T>C	ENSP00000419045.2:n.453+48T>C
ENST00000536224.2:c.453+48T>C	ENSP00000445246.2:n.453+48T>C
ENST00000543643.6:c.453+48T>C	ENSP00000444011.2:n.453+48T>C
ENST00000622544.4:c.453+48T>C	ENSP00000477796.1:n.453+48T>C
NM_000161.2:c.453+48T>C	NP_000152.1:n.453+48T>C
NM_001024024.1:c.453+48T>C	NP_001019195.1:n.453+48T>C
NM_001024070.1:c.453+48T>C	NP_001019241.1:n.453+48T>C
NM_001024071.1:c.453+48T>C	NP_001019242.1:n.453+48T>C
XM_005267530.1:c.453+48T>C	XP_005267587.1:n.453+48T>C
XM_011536643.1:c.453+48T>C	XP_011534945.1:n.453+48T>C
XM_017021218.1:c.159+48T>C	XP_016876707.1:n.159+48T>C
NM_000161.3:c.453+48T>C MANE Select	NP_000152.1:n.453+48T>C
NM_001024070.2:c.453+48T>C	NP_001019241.1:n.453+48T>C
NM_001024071.2:c.453+48T>C	NP_001019242.1:n.453+48T>C
NM_001024024.2:c.453+48T>C	NP_001019195.1:n.453+48T>C