Canonical Allele Identifier: CA458161991

Gene: BPGM

Linked Data

• MyVariant Identifiers: chr7:g.134346430A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.134661678A>C , CM000669.2:g.134661678A>C	GRCh38
NC_000007.13:g.134346430A>C , CM000669.1:g.134346430A>C	GRCh37
NC_000007.12:g.133996970A>C	NCBI36
NG_012921.1:g.19900A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344924.8:c.171A>C MANE Select	ENSP00000342032.3:p.Thr57=
ENST00000344924.7:c.171A>C	ENSP00000342032.3:p.Thr57=
ENST00000393132.2:c.171A>C	ENSP00000376840.2:p.Thr57=
ENST00000418040.5:c.171A>C	ENSP00000399838.1:p.Thr57=
ENST00000443095.1:c.171A>C	ENSP00000403050.1:p.Thr57=
NM_001293085.1:c.171A>C	NP_001280014.1:p.Thr57=
NM_001724.4:c.171A>C	NP_001715.1:p.Thr57=
NM_199186.2:c.171A>C	NP_954655.1:p.Thr57=
XM_011516527.1:c.171A>C	XP_011514829.1:p.Thr57=
XR_928017.1:n.6821-543T>G
XM_011516527.2:c.171A>C	XP_011514829.1:p.Thr57=
NM_001724.5:c.171A>C MANE Select	NP_001715.1:p.Thr57=
NM_001293085.2:c.171A>C	NP_001280014.1:p.Thr57=
NM_199186.3:c.171A>C	NP_954655.1:p.Thr57=