Canonical Allele Identifier: CA341551132

Gene: EPS8L3 GSTM5

Linked Data

• MyVariant Identifiers: chr1:g.110299681C>G (hg19) ; chr1:g.109757059C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109757059C>G , CM000663.2:g.109757059C>G	GRCh38
NC_000001.10:g.110299681C>G , CM000663.1:g.110299681C>G	GRCh37
NC_000001.9:g.110101204C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361965.9:c.1076G>C (EPS8L3) MANE Select	ENSP00000355255.4:p.Ser359Thr
ENST00000361852.8:c.1076G>C (EPS8L3)	ENSP00000354551.4:p.Ser359Thr
ENST00000361965.8:c.1076G>C (EPS8L3)	ENSP00000355255.4:p.Ser359Thr
ENST00000369805.7:c.1079G>C (EPS8L3)	ENSP00000358820.3:p.Ser360Thr
ENST00000429410.2:n.83-18013C>G (GSTM5)
ENST00000472325.5:c.*1045G>C (EPS8L3)	ENSP00000483789.1:n.*1045G>C
NM_024526.3:c.1076G>C (EPS8L3)	NP_078802.2:p.Ser359Thr
NM_133181.3:c.1076G>C (EPS8L3)	NP_573444.2:p.Ser359Thr
NM_139053.2:c.1079G>C (EPS8L3)	NP_620641.1:p.Ser360Thr
XM_011542127.1:c.1346G>C (EPS8L3)	XP_011540429.1:p.Ser449Thr
XM_011542128.1:c.1343G>C (EPS8L3)	XP_011540430.1:p.Ser448Thr
XM_011542129.1:c.1322G>C (EPS8L3)	XP_011540431.1:p.Ser441Thr
XM_011542130.1:c.1346G>C (EPS8L3)	XP_011540432.1:p.Ser449Thr
XM_011542131.1:c.1346G>C (EPS8L3)	XP_011540433.1:p.Ser449Thr
XM_011542132.1:c.1103G>C (EPS8L3)	XP_011540434.1:p.Ser368Thr
XM_011542133.1:c.1100G>C (EPS8L3)	XP_011540435.1:p.Ser367Thr
XM_011542134.1:c.1001G>C (EPS8L3)	XP_011540436.1:p.Ser334Thr
XM_011542135.1:c.1001G>C (EPS8L3)	XP_011540437.1:p.Ser334Thr
XM_011542136.1:c.977G>C (EPS8L3)	XP_011540438.1:p.Ser326Thr
XR_946755.1:n.1524G>C (EPS8L3)
XR_946756.1:n.1525G>C (EPS8L3)
NM_001319952.1:c.977G>C (EPS8L3)	NP_001306881.1:p.Ser326Thr
XM_011542132.2:c.1103G>C (EPS8L3)	XP_011540434.1:p.Ser368Thr
XM_011542133.2:c.1100G>C (EPS8L3)	XP_011540435.1:p.Ser367Thr
XM_011542134.3:c.1001G>C (EPS8L3)	XP_011540436.1:p.Ser334Thr
XM_011542135.3:c.1001G>C (EPS8L3)	XP_011540437.1:p.Ser334Thr
XM_017002327.2:c.1103G>C (EPS8L3)	XP_016857816.1:p.Ser368Thr
XM_017002328.2:c.1103G>C (EPS8L3)	XP_016857817.1:p.Ser368Thr
XM_017002329.2:c.1079G>C (EPS8L3)	XP_016857818.1:p.Ser360Thr
XR_001737406.2:n.1252G>C (EPS8L3)
XR_001737407.2:n.1252G>C (EPS8L3)
NM_001319952.2:c.977G>C (EPS8L3)	NP_001306881.1:p.Ser326Thr
NM_024526.4:c.1076G>C (EPS8L3)	NP_078802.2:p.Ser359Thr
NM_133181.4:c.1076G>C (EPS8L3) MANE Select	NP_573444.2:p.Ser359Thr
NM_139053.3:c.1079G>C (EPS8L3)	NP_620641.1:p.Ser360Thr