Canonical Allele Identifier: CA1703602916

Gene: PGAM2 DBNL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44062734G= , CM000669.2:g.44062734G=	GRCh38
NC_000007.13:g.44102333G= , CM000669.1:g.44102333G=	GRCh37
NC_000007.12:g.44068858G=	NCBI36
NG_013016.1:g.7854C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297283.4:c.*30C= (PGAM2) MANE Select	ENSP00000297283.3:n.*30C=
ENST00000448521.6:c.*1818G= (DBNL) MANE Select	ENSP00000411701.1:n.*1818G=
ENST00000297283.3:c.*30C= (PGAM2)	ENSP00000297283.3:n.*30C=
ENST00000432854.5:c.2896G= (DBNL)
NM_000290.3:c.*30C= (PGAM2)	NP_000281.2:n.*30C=
NM_000290.4:c.*30C= (PGAM2) MANE Select	NP_000281.2:n.*30C=
NM_001014436.3:c.*1818G= (DBNL) MANE Select	NP_001014436.1:n.*1818G=
NM_001122956.2:c.*1818G= (DBNL)	NP_001116428.1:n.*1818G=
NM_001284313.2:c.*1818G= (DBNL)	NP_001271242.1:n.*1818G=
NM_001362723.2:c.*1818G= (DBNL)	NP_001349652.1:n.*1818G=
NM_014063.7:c.*1818G= (DBNL)	NP_054782.2:n.*1818G=
NM_001284315.2:c.*1818G= (DBNL)	NP_001271244.1:n.*1818G=