Canonical Allele Identifier: CA1621871796

Gene: MDGA1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37661874G= , CM000668.2:g.37661874G=	GRCh38
NC_000006.11:g.37629650G= , CM000668.1:g.37629650G=	GRCh37
NC_000006.10:g.37737628G=	NCBI36
NG_051764.1:g.41117C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434837.8:c.207+2093C= MANE Select	ENSP00000402584.2:n.207+2093C=
ENST00000650466.1:c.207+2093C=	ENSP00000498018.1:n.207+2093C=
ENST00000681439.1:c.39+2093C=	ENSP00000506441.1:n.39+2093C=
ENST00000681472.1:c.207+2093C=	ENSP00000506519.1:n.207+2093C=
ENST00000434837.7:c.207+2093C=	ENSP00000402584.2:n.207+2093C=
ENST00000478143.2:n.23+2093C=
ENST00000505425.5:c.207+2093C=	ENSP00000422042.1:n.207+2093C=
ENST00000508399.1:c.39+2093C=	ENSP00000427645.1:n.39+2093C=
ENST00000515437.5:c.39+2093C=	ENSP00000421510.1:n.39+2093C=
NM_153487.3:c.207+2093C=	NP_705691.1:n.207+2093C=
XM_006715056.2:c.207+2093C=	XP_006715119.1:n.207+2093C=
XM_006715057.2:c.207+2093C=	XP_006715120.1:n.207+2093C=
XR_926140.1:n.396+2093C=
XR_926141.1:n.396+2093C=
XR_926142.1:n.396+2093C=
XM_006715056.3:c.207+2093C=	XP_006715119.1:n.207+2093C=
XM_017010734.1:c.207+2093C=	XP_016866223.1:n.207+2093C=
XR_926140.2:n.330+2093C=
XR_926141.2:n.330+2093C=
XR_926142.2:n.330+2093C=
NM_153487.4:c.207+2093C= MANE Select	NP_705691.1:n.207+2093C=