Canonical Allele Identifier: CA706297237

Gene: MDGA2

Linked Data

• dbSNP Id: rs1186344843
• gnomAD v3: 14-47355251-TG-T
• gnomAD v4: 14-47355251-TG-T
• MyVariant Identifiers: chr14:g.47824455del (hg19) ; chr14:g.47355252del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.47355252del , CM000676.2:g.47355252del	GRCh38
NC_000014.8:g.47824455del , CM000676.1:g.47824455del	GRCh37
NC_000014.7:g.46894205del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399232.8:c.281-53702del MANE Select	ENSP00000382178.4:n.281-53702del
ENST00000399232.6:c.74-53702del	ENSP00000382178.3:n.74-53702del
ENST00000557238.5:c.-614-53702del	ENSP00000452593.1:n.-614-53702del
NM_001113498.2:c.74-53702del	NP_001106970.3:n.74-53702del
XM_011536520.1:c.281-53702del	XP_011534822.1:n.281-53702del
XM_011536521.1:c.281-53702del	XP_011534823.1:n.281-53702del
XM_011536522.1:c.281-53702del	XP_011534824.1:n.281-53702del
XM_011536523.1:c.281-53702del	XP_011534825.1:n.281-53702del
XM_011536522.3:c.281-53702del	XP_011534824.1:n.281-53702del
XM_017021061.2:c.281-53702del	XP_016876550.1:n.281-53702del
XR_001750175.2:n.801-53702del
NM_001113498.3:c.281-53702del MANE Select	NP_001106970.4:n.281-53702del