Canonical Allele Identifier: CA3488127

Gene: GRXCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145872921G>C , CM000667.2:g.145872921G>C	GRCh38
NC_000005.9:g.145252484G>C , CM000667.1:g.145252484G>C	GRCh37
NC_000005.8:g.145232677G>C	NCBI36
NG_034161.1:g.5048C>G
NG_034161.2:g.5094C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001080516.2:c.48C>G MANE Select	NP_001073985.1:p.Pro16=
ENST00000377976.3:c.48C>G MANE Select	ENSP00000367214.1:p.Pro16=
NM_001080516.1:c.48C>G	NP_001073985.1:p.Pro16=
ENST00000377976.1:c.48C>G	ENSP00000367214.1:p.Pro16=
ENST00000639411.1:c.-69-6193C>G	ENSP00000491860.1:n.-69-6193C>G
XM_011537674.1:c.48C>G	XP_011535976.1:p.Pro16=
XM_011537675.1:c.67-6193C>G	XP_011535977.1:n.67-6193C>G
XM_011537676.1:c.49-6193C>G	XP_011535978.1:n.49-6193C>G
XM_017009708.1:c.49-6193C>G	XP_016865197.1:n.49-6193C>G