Canonical Allele Identifier: CA2134516318

Gene: MDGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.46985783G= , CM000676.2:g.46985783G=	GRCh38
NC_000014.8:g.47454986G= , CM000676.1:g.47454986G=	GRCh37
NC_000014.7:g.46524736G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001113498.3:c.1820-28140C= MANE Select	NP_001106970.4:n.1820-28140C=
ENST00000399232.8:c.1820-28140C= MANE Select	ENSP00000382178.4:n.1820-28140C=
NM_001113498.2:c.1613-28140C=	NP_001106970.3:n.1613-28140C=
NM_182830.4:c.926-28140C=	NP_878250.2:n.926-28140C=
ENST00000357362.7:c.926-28140C=	ENSP00000349925.3:n.926-28140C=
ENST00000399232.6:c.1613-28140C=	ENSP00000382178.3:n.1613-28140C=
ENST00000426342.5:c.1223-28140C=	ENSP00000405456.2:n.1223-28140C=
ENST00000426342.7:c.1223-28140C=	ENSP00000405456.4:n.1223-28140C=
ENST00000557238.5:c.*198-28140C=	ENSP00000452593.1:n.*198-28140C=
XM_011536519.1:c.1685-28140C=	XP_011534821.1:n.1685-28140C=
XM_011536519.2:c.1685-28140C=	XP_011534821.1:n.1685-28140C=
XM_011536520.1:c.1820-28140C=	XP_011534822.1:n.1820-28140C=
XM_011536521.1:c.1526-65623C=	XP_011534823.1:n.1526-65623C=
XM_011536522.1:c.*37+8861C=	XP_011534824.1:n.*37+8861C=
XM_011536522.3:c.*37+8861C=	XP_011534824.1:n.*37+8861C=
XM_011536524.1:c.458-28140C=	XP_011534826.1:n.458-28140C=
XM_011536525.1:c.293-28140C=	XP_011534827.1:n.293-28140C=
XM_011536525.2:c.293-28140C=	XP_011534827.1:n.293-28140C=
XM_017021060.1:c.458-28140C=	XP_016876549.1:n.458-28140C=
XR_001750175.2:n.2314-28140C=