Canonical Allele Identifier: CA15450578

Gene: GMPR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.16287961G>A , CM000668.2:g.16287961G>A	GRCh38
NC_000006.11:g.16288192G>A , CM000668.1:g.16288192G>A	GRCh37
NC_000006.10:g.16396171G>A	NCBI36
NG_013303.1:g.54382G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259727.5:c.697+2126G>A MANE Select	ENSP00000259727.4:n.697+2126G>A
ENST00000259727.4:c.697+2126G>A	ENSP00000259727.4:n.697+2126G>A
ENST00000543191.5:n.192+2126G>A
NM_006877.3:c.697+2126G>A	NP_006868.3:n.697+2126G>A
XM_011514508.1:c.698-1465G>A	XP_011512810.1:n.698-1465G>A
XM_011514508.2:c.698-1465G>A	XP_011512810.1:n.698-1465G>A
NM_006877.4:c.697+2126G>A MANE Select	NP_006868.3:n.697+2126G>A