Canonical Allele Identifier: CA261045982

Gene: MDGA2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.47305298G>T , CM000676.2:g.47305298G>T	GRCh38
NC_000014.8:g.47774501G>T , CM000676.1:g.47774501G>T	GRCh37
NC_000014.7:g.46844251G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399232.8:c.281-3748C>A MANE Select	ENSP00000382178.4:n.281-3748C>A
ENST00000357362.7:c.-614-3748C>A	ENSP00000349925.3:n.-614-3748C>A
ENST00000399232.6:c.74-3748C>A	ENSP00000382178.3:n.74-3748C>A
ENST00000472499.2:n.111C>A
ENST00000482848.7:c.-609-3748C>A	ENSP00000434991.2:n.-609-3748C>A
ENST00000486952.2:c.146-3748C>A	ENSP00000452515.1:n.146-3748C>A
ENST00000557238.5:c.-614-3748C>A	ENSP00000452593.1:n.-614-3748C>A
NM_001113498.2:c.74-3748C>A	NP_001106970.3:n.74-3748C>A
NM_182830.4:c.-609-3748C>A	NP_878250.2:n.-609-3748C>A
NR_103766.1:n.150-3748C>A
XM_011536519.1:c.146-3748C>A	XP_011534821.1:n.146-3748C>A
XM_011536520.1:c.281-3748C>A	XP_011534822.1:n.281-3748C>A
XM_011536521.1:c.281-3748C>A	XP_011534823.1:n.281-3748C>A
XM_011536522.1:c.281-3748C>A	XP_011534824.1:n.281-3748C>A
XM_011536523.1:c.281-3748C>A	XP_011534825.1:n.281-3748C>A
XM_011536519.2:c.146-3748C>A	XP_011534821.1:n.146-3748C>A
XM_011536522.3:c.281-3748C>A	XP_011534824.1:n.281-3748C>A
XM_017021061.2:c.281-3748C>A	XP_016876550.1:n.281-3748C>A
XR_001750175.2:n.801-3748C>A
NM_001113498.3:c.281-3748C>A MANE Select	NP_001106970.4:n.281-3748C>A
NR_103766.2:n.150-3748C>A