Canonical Allele Identifier: CA418785847

Gene: GLMN

Linked Data

• gnomAD v4: 1-92266426-A-G
• COSMIC: COSM913294
• MyVariant Identifiers: chr1:g.92731983A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266426A>G , CM000663.2:g.92266426A>G	GRCh38
NC_000001.10:g.92731983A>G , CM000663.1:g.92731983A>G	GRCh37
NC_000001.9:g.92504571A>G	NCBI36
NG_009796.1:g.37584T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370360.8:c.1207T>C MANE Select	ENSP00000359385.3:p.Leu403=
ENST00000370360.7:c.1207T>C	ENSP00000359385.3:p.Leu403=
ENST00000463560.1:c.562+114T>C
ENST00000495106.5:c.1207T>C	ENSP00000436829.1:p.Leu403=
ENST00000495852.6:c.430T>C	ENSP00000469157.2:p.Leu144=
NM_053274.2:c.1207T>C	NP_444504.1:p.Leu403=
XM_005270400.1:c.1165T>C	XP_005270457.1:p.Leu389=
XM_005270401.2:c.1081T>C	XP_005270458.1:p.Leu361=
XM_006710309.1:c.706T>C	XP_006710372.1:p.Leu236=
XM_011540544.1:c.1207T>C	XP_011538846.1:p.Leu403=
XM_011540545.1:c.1207T>C	XP_011538847.1:p.Leu403=
XM_011540546.1:c.1207T>C	XP_011538848.1:p.Leu403=
XR_946529.1:n.1309+114T>C
NM_001319683.1:c.1165T>C	NP_001306612.1:p.Leu389=
NR_135089.1:n.1322T>C
XM_005270401.3:c.1081T>C	XP_005270458.1:p.Leu361=
XM_006710309.2:c.706T>C	XP_006710372.1:p.Leu236=
XM_011540546.2:c.1207T>C	XP_011538848.1:p.Leu403=
XM_017000137.1:c.1306T>C	XP_016855626.1:p.Leu436=
XM_017000138.1:c.1264T>C	XP_016855627.1:p.Leu422=
XM_017000139.1:c.1293+114T>C	XP_016855628.1:n.1293+114T>C
XM_017000140.1:c.1180T>C	XP_016855629.1:p.Leu394=
XM_017000141.1:c.1194+114T>C	XP_016855630.1:n.1194+114T>C
XM_017000142.1:c.664T>C	XP_016855631.1:p.Leu222=
XM_017000143.1:c.664T>C	XP_016855632.1:p.Leu222=
XM_017000144.1:c.436T>C	XP_016855633.1:p.Leu146=
XR_002959248.1:n.1677+114T>C
XR_002959249.1:n.1309+114T>C
NM_053274.3:c.1207T>C MANE Select	NP_444504.1:p.Leu403=
NM_001319683.2:c.1165T>C	NP_001306612.1:p.Leu389=
NR_135089.2:n.1300T>C