Canonical Allele Identifier: CA614285265

Gene: GCH1

Linked Data

• dbSNP Id: rs1314759904
• gnomAD v2: 14-55324611-T-G
• gnomAD v3: 14-54857893-T-G
• gnomAD v4: 14-54857893-T-G
• MyVariant Identifiers: chr14:g.55324611T>G (hg19) ; chr14:g.54857893T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54857893T>G , CM000676.2:g.54857893T>G	GRCh38
NC_000014.8:g.55324611T>G , CM000676.1:g.55324611T>G	GRCh37
NC_000014.7:g.54394361T>G	NCBI36
NG_008647.1:g.49932A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.509+1788A>C MANE Select	ENSP00000419045.2:n.509+1788A>C
ENST00000254299.8:n.657+1788A>C
ENST00000395514.5:c.509+1788A>C	ENSP00000378890.1:n.509+1788A>C
ENST00000395521.6:n.292+1788A>C
ENST00000491895.6:c.509+1788A>C	ENSP00000419045.2:n.509+1788A>C
ENST00000536224.2:c.509+1788A>C	ENSP00000445246.2:n.509+1788A>C
ENST00000543643.6:c.509+1788A>C	ENSP00000444011.2:n.509+1788A>C
ENST00000622544.4:c.509+1788A>C	ENSP00000477796.1:n.509+1788A>C
NM_000161.2:c.509+1788A>C	NP_000152.1:n.509+1788A>C
NM_001024024.1:c.509+1788A>C	NP_001019195.1:n.509+1788A>C
NM_001024070.1:c.509+1788A>C	NP_001019241.1:n.509+1788A>C
NM_001024071.1:c.509+1788A>C	NP_001019242.1:n.509+1788A>C
XM_005267530.1:c.509+1788A>C	XP_005267587.1:n.509+1788A>C
XM_011536643.1:c.510-1126A>C	XP_011534945.1:n.510-1126A>C
XM_017021218.1:c.215+1788A>C	XP_016876707.1:n.215+1788A>C
NM_000161.3:c.509+1788A>C MANE Select	NP_000152.1:n.509+1788A>C
NM_001024070.2:c.509+1788A>C	NP_001019241.1:n.509+1788A>C
NM_001024071.2:c.509+1788A>C	NP_001019242.1:n.509+1788A>C
NM_001024024.2:c.509+1788A>C	NP_001019195.1:n.509+1788A>C