Canonical Allele Identifier: CA352827258

Gene: GMPPB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49722054G>A , CM000665.2:g.49722054G>A	GRCh38
NC_000003.11:g.49759487G>A , CM000665.1:g.49759487G>A	GRCh37
NC_000003.10:g.49734491G>A	NCBI36
NG_011603.1:g.37498G>A
NG_033731.1:g.6921C>T
NG_033731.2:g.6921C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021971.4:c.862C>T MANE Select	NP_068806.2:p.Arg288Trp
ENST00000308388.7:c.862C>T MANE Select	ENSP00000311130.6:p.Arg288Trp
NM_013334.3:c.862C>T	NP_037466.2:p.Arg288Trp
NM_013334.4:c.862C>T	NP_037466.3:p.Arg288Trp
NM_021971.2:c.862C>T	NP_068806.1:p.Arg288Trp
ENST00000308375.10:c.862C>T	ENSP00000309092.6:p.Arg288Trp
ENST00000308388.6:c.862C>T	ENSP00000311130.6:p.Arg288Trp
ENST00000480687.5:c.862C>T	ENSP00000418565.1:p.Arg288Trp
ENST00000481959.2:n.1435C>T
ENST00000495627.2:c.970C>T	ENSP00000503768.1:p.Arg324Trp
ENST00000677393.1:c.655C>T	ENSP00000503880.1:p.Arg219Trp
ENST00000678010.1:c.496C>T	ENSP00000503176.1:p.Arg166Trp
ENST00000678208.1:n.1296C>T
ENST00000678853.1:c.*153C>T	ENSP00000504692.1:n.*153C>T