Canonical Allele Identifier: CA2405310738

Gene: MGAT3

Genomic Alleles

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

Transcript Alleles

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