Canonical Allele Identifier: CA433850870

Gene: GMPPB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49722327G>A , CM000665.2:g.49722327G>A	GRCh38
NC_000003.11:g.49759760G>A , CM000665.1:g.49759760G>A	GRCh37
NC_000003.10:g.49734764G>A	NCBI36
NG_011603.1:g.37771G>A
NG_033731.1:g.6648C>T
NG_033731.2:g.6648C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021971.4:c.672C>T MANE Select	NP_068806.2:p.Asp224=
ENST00000308388.7:c.672C>T MANE Select	ENSP00000311130.6:p.Asp224=
NM_013334.3:c.672C>T	NP_037466.2:p.Asp224=
NM_013334.4:c.672C>T	NP_037466.3:p.Asp224=
NM_021971.2:c.672C>T	NP_068806.1:p.Asp224=
ENST00000308375.10:c.672C>T	ENSP00000309092.6:p.Asp224=
ENST00000308388.6:c.672C>T	ENSP00000311130.6:p.Asp224=
ENST00000480687.5:c.672C>T	ENSP00000418565.1:p.Asp224=
ENST00000481959.2:n.1245C>T
ENST00000495627.2:c.780C>T	ENSP00000503768.1:p.Asp260=
ENST00000677393.1:c.562-180C>T	ENSP00000503880.1:n.562-180C>T
ENST00000678010.1:c.403-180C>T	ENSP00000503176.1:n.403-180C>T
ENST00000678208.1:n.1106C>T
ENST00000678853.1:c.434C>T	ENSP00000504692.1:p.Thr145Ile