Canonical Allele Identifier: CA2405310739

Gene: MGAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39463164C>G , CM000684.2:g.39463164C>G	GRCh38
NC_000022.10:g.39859169C>G , CM000684.1:g.39859169C>G	GRCh37
NC_000022.9:g.38189115C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341184.7:c.-2+5607C>G MANE Select	ENSP00000345270.6:n.-2+5607C>G
ENST00000341184.6:c.-2+5607C>G	ENSP00000345270.6:n.-2+5607C>G
NM_002409.4:c.-2+5607C>G	NP_002400.3:n.-2+5607C>G
XM_005261608.3:c.125+8495C>G	XP_005261665.1:n.125+8495C>G
XM_011530191.1:c.-2+15867C>G	XP_011528493.1:n.-2+15867C>G
XM_011530194.1:c.-2+6759C>G	XP_011528496.1:n.-2+6759C>G
XM_005261608.5:c.125+8495C>G	XP_005261665.1:n.125+8495C>G
XM_011530191.3:c.-2+15867C>G	XP_011528493.1:n.-2+15867C>G
XM_011530194.2:c.-2+6759C>G	XP_011528496.1:n.-2+6759C>G
NM_002409.5:c.-2+5607C>G MANE Select	NP_002400.3:n.-2+5607C>G