Canonical Allele Identifier: CA362800558
Gene: GMPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16290539A>C , CM000668.2:g.16290539A>C GRCh38
NC_000006.11:g.16290770A>C , CM000668.1:g.16290770A>C GRCh37
NC_000006.10:g.16398749A>C NCBI36
NG_013303.1:g.56960A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000259727.5:c.775A>C MANE Select ENSP00000259727.4:p.Asn259His
ENST00000259727.4:c.775A>C ENSP00000259727.4:p.Asn259His
ENST00000540478.1:n.595A>C
ENST00000543191.5:n.270A>C
ENST00000544145.1:n.129A>C
NM_006877.3:c.775A>C NP_006868.3:p.Asn259His
XM_011514508.1:c.918A>C XP_011512810.1:p.Gly306=
XM_011514508.2:c.918A>C XP_011512810.1:p.Gly306=
NM_006877.4:c.775A>C MANE Select NP_006868.3:p.Asn259His