Canonical Allele Identifier: CA369472355

Gene: BPGM

Linked Data

• gnomAD v4: 7-134661764-G-T
• MyVariant Identifiers: chr7:g.134346516G>T (hg19) ; chr7:g.134661764G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.134661764G>T , CM000669.2:g.134661764G>T	GRCh38
NC_000007.13:g.134346516G>T , CM000669.1:g.134346516G>T	GRCh37
NC_000007.12:g.133997056G>T	NCBI36
NG_012921.1:g.19986G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344924.8:c.257G>T MANE Select	ENSP00000342032.3:p.Arg86Leu
ENST00000344924.7:c.257G>T	ENSP00000342032.3:p.Arg86Leu
ENST00000393132.2:c.257G>T	ENSP00000376840.2:p.Arg86Leu
ENST00000418040.5:c.257G>T	ENSP00000399838.1:p.Arg86Leu
NM_001293085.1:c.257G>T	NP_001280014.1:p.Arg86Leu
NM_001724.4:c.257G>T	NP_001715.1:p.Arg86Leu
NM_199186.2:c.257G>T	NP_954655.1:p.Arg86Leu
XM_011516527.1:c.257G>T	XP_011514829.1:p.Arg86Leu
XR_928017.1:n.6821-629C>A
XM_011516527.2:c.257G>T	XP_011514829.1:p.Arg86Leu
NM_001724.5:c.257G>T MANE Select	NP_001715.1:p.Arg86Leu
NM_001293085.2:c.257G>T	NP_001280014.1:p.Arg86Leu
NM_199186.3:c.257G>T	NP_954655.1:p.Arg86Leu