Canonical Allele Identifier: CA260489023

Gene: MDGA2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.46934481A>T , CM000676.2:g.46934481A>T	GRCh38
NC_000014.8:g.47403684A>T , CM000676.1:g.47403684A>T	GRCh37
NC_000014.7:g.46473434A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399232.8:c.2090-14321T>A MANE Select	ENSP00000382178.4:n.2090-14321T>A
ENST00000426342.7:c.1493-14321T>A	ENSP00000405456.4:n.1493-14321T>A
ENST00000357362.7:c.1196-14321T>A	ENSP00000349925.3:n.1196-14321T>A
ENST00000399232.6:c.1883-14321T>A	ENSP00000382178.3:n.1883-14321T>A
ENST00000426342.5:c.1493-14321T>A	ENSP00000405456.2:n.1493-14321T>A
ENST00000557238.5:c.*468-14321T>A	ENSP00000452593.1:n.*468-14321T>A
NM_001113498.2:c.1883-14321T>A	NP_001106970.3:n.1883-14321T>A
NM_182830.4:c.1196-14321T>A	NP_878250.2:n.1196-14321T>A
XM_011536519.1:c.1955-14321T>A	XP_011534821.1:n.1955-14321T>A
XM_011536520.1:c.2090-14321T>A	XP_011534822.1:n.2090-14321T>A
XM_011536521.1:c.1526-14321T>A	XP_011534823.1:n.1526-14321T>A
XM_011536524.1:c.728-14321T>A	XP_011534826.1:n.728-14321T>A
XM_011536525.1:c.563-14321T>A	XP_011534827.1:n.563-14321T>A
XM_011536519.2:c.1955-14321T>A	XP_011534821.1:n.1955-14321T>A
XM_011536525.2:c.563-14321T>A	XP_011534827.1:n.563-14321T>A
XM_017021060.1:c.728-14321T>A	XP_016876549.1:n.728-14321T>A
XR_001750175.2:n.2584-14321T>A
NM_001113498.3:c.2090-14321T>A MANE Select	NP_001106970.4:n.2090-14321T>A