Canonical Allele Identifier: CA15087508
Gene: MGST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165647351T>C , CM000663.2:g.165647351T>C GRCh38
NC_000001.10:g.165616588T>C , CM000663.1:g.165616588T>C GRCh37
NC_000001.9:g.163883212T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367889.8:c.-7-2490T>C MANE Select ENSP00000356864.3:n.-7-2490T>C
ENST00000367883.3:c.36-2490T>C ENSP00000356858.1:n.36-2490T>C
ENST00000367884.6:c.-7-2490T>C ENSP00000356859.1:n.-7-2490T>C
ENST00000367885.5:c.36-2490T>C ENSP00000356860.1:n.36-2490T>C
ENST00000367888.8:c.-7-2490T>C ENSP00000356863.4:n.-7-2490T>C
ENST00000367889.7:c.-7-2490T>C ENSP00000356864.3:n.-7-2490T>C
ENST00000461308.1:n.69-2490T>C
ENST00000461759.1:n.1691T>C
ENST00000488688.1:n.37-2490T>C
ENST00000495447.5:n.56-2404T>C
ENST00000627653.1:c.36-2490T>C ENSP00000487151.1:n.36-2490T>C
NM_004528.3:c.-7-2490T>C NP_004519.1:n.-7-2490T>C
XM_005245174.2:c.-7-2490T>C XP_005245231.2:n.-7-2490T>C
XM_005245174.3:c.-7-2490T>C XP_005245231.2:n.-7-2490T>C
NM_004528.4:c.-7-2490T>C MANE Select NP_004519.1:n.-7-2490T>C
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