Canonical Allele Identifier: CA376375933

Gene: YME1L1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27136371G>C , CM000672.2:g.27136371G>C	GRCh38
NC_000010.10:g.27425300G>C , CM000672.1:g.27425300G>C	GRCh37
NC_000010.9:g.27465306G>C	NCBI36
NG_047122.1:g.23908C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376016.8:c.445C>G MANE Select	ENSP00000365184.3:p.Arg149Gly
ENST00000326799.7:c.616C>G	ENSP00000318480.3:p.Arg206Gly
ENST00000375972.7:c.616C>G	ENSP00000365139.4:p.Arg206Gly
ENST00000376016.7:c.445C>G	ENSP00000365184.3:p.Arg149Gly
ENST00000396296.7:c.421C>G	ENSP00000379590.3:p.Arg141Gly
ENST00000427324.5:c.346C>G	ENSP00000398713.1:p.Arg116Gly
ENST00000491542.6:c.169-1390C>G	ENSP00000473557.1:n.169-1390C>G
ENST00000613434.4:c.346C>G	ENSP00000481724.1:p.Arg116Gly
NM_001253866.1:c.346C>G	NP_001240795.1:p.Arg116Gly
NM_014263.3:c.445C>G	NP_055078.1:p.Arg149Gly
NM_139312.2:c.616C>G	NP_647473.1:p.Arg206Gly
XM_011519300.1:c.517C>G	XP_011517602.1:p.Arg173Gly
XM_011519300.3:c.517C>G	XP_011517602.1:p.Arg173Gly
NM_014263.4:c.445C>G MANE Select	NP_055078.1:p.Arg149Gly
NM_139312.3:c.616C>G	NP_647473.1:p.Arg206Gly
NM_001253866.2:c.346C>G	NP_001240795.1:p.Arg116Gly