Canonical Allele Identifier: CA12698590

Gene: PGAM2 DBNL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44064620A>G , CM000669.2:g.44064620A>G	GRCh38
NC_000007.13:g.44104219A>G , CM000669.1:g.44104219A>G	GRCh37
NC_000007.12:g.44070744A>G	NCBI36
NG_013016.1:g.5968T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000290.4:c.595+212T>C (PGAM2) MANE Select	NP_000281.2:n.595+212T>C
NM_001014436.3:c.*3704A>G (DBNL) MANE Select	NP_001014436.1:n.*3704A>G
ENST00000297283.4:c.595+212T>C (PGAM2) MANE Select	ENSP00000297283.3:n.595+212T>C
ENST00000448521.6:c.*3704A>G (DBNL) MANE Select	ENSP00000411701.1:n.*3704A>G
NM_000290.3:c.595+212T>C (PGAM2)	NP_000281.2:n.595+212T>C
NM_001122956.2:c.*3704A>G (DBNL)	NP_001116428.1:n.*3704A>G
NM_001284313.2:c.*3704A>G (DBNL)	NP_001271242.1:n.*3704A>G
NM_001284315.2:c.*3704A>G (DBNL)	NP_001271244.1:n.*3704A>G
NM_001362723.2:c.*3704A>G (DBNL)	NP_001349652.1:n.*3704A>G
NM_014063.7:c.*3704A>G (DBNL)	NP_054782.2:n.*3704A>G
ENST00000297283.3:c.595+212T>C (PGAM2)	ENSP00000297283.3:n.595+212T>C
ENST00000432854.5:c.4782A>G (DBNL)
XM_011515426.1:c.414+496T>C (PGAM2)	XP_011513728.1:n.414+496T>C