Canonical Allele Identifier: CA1205465748

Gene: MPC2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167933804T= , CM000663.2:g.167933804T=	GRCh38
NC_000001.10:g.167903042T= , CM000663.1:g.167903042T=	GRCh37
NC_000001.9:g.166169666T=	NCBI36
NG_053062.1:g.2566T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271373.9:c.109+1929A= MANE Select	ENSP00000271373.4:n.109+1929A=
ENST00000271373.8:c.109+1929A=	ENSP00000271373.4:n.109+1929A=
ENST00000367846.8:c.109+1929A=	ENSP00000356820.4:n.109+1929A=
ENST00000458574.1:c.109+1929A=	ENSP00000392874.1:n.109+1929A=
NM_001143674.3:c.109+1929A=	NP_001137146.1:n.109+1929A=
NM_015415.3:c.109+1929A=	NP_056230.1:n.109+1929A=
NR_026550.2:n.469+1929A=
XM_006711266.2:c.109+1929A=	XP_006711329.1:n.109+1929A=
XM_006711266.3:c.109+1929A=	XP_006711329.1:n.109+1929A=
NM_001143674.4:c.109+1929A= MANE Select	NP_001137146.1:n.109+1929A=
NR_026550.3:n.264+1929A=