Canonical Allele Identifier: CA4494671
Gene: BPGM HGNC NCBI

Linked Data

dbSNP Id: rs781222092

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.134661776G>T , CM000669.2:g.134661776G>T GRCh38
NC_000007.13:g.134346528G>T , CM000669.1:g.134346528G>T GRCh37
NC_000007.12:g.133997068G>T NCBI36
NG_012921.1:g.19998G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344924.8:c.269G>T MANE Select ENSP00000342032.3:p.Arg90Leu
ENST00000344924.7:c.269G>T ENSP00000342032.3:p.Arg90Leu
ENST00000393132.2:c.269G>T ENSP00000376840.2:p.Arg90Leu
ENST00000418040.5:c.269G>T ENSP00000399838.1:p.Arg90Leu
NM_001293085.1:c.269G>T NP_001280014.1:p.Arg90Leu
NM_001724.4:c.269G>T NP_001715.1:p.Arg90Leu
NM_199186.2:c.269G>T NP_954655.1:p.Arg90Leu
XM_011516527.1:c.269G>T XP_011514829.1:p.Arg90Leu
XR_928017.1:n.6821-641C>A
XM_011516527.2:c.269G>T XP_011514829.1:p.Arg90Leu
NM_001724.5:c.269G>T MANE Select NP_001715.1:p.Arg90Leu
NM_001293085.2:c.269G>T NP_001280014.1:p.Arg90Leu
NM_199186.3:c.269G>T NP_954655.1:p.Arg90Leu