Canonical Allele Identifier: CA418785860

Gene: GLMN

Linked Data

• gnomAD v4: 1-92266450-A-G
• MyVariant Identifiers: chr1:g.92732007A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266450A>G , CM000663.2:g.92266450A>G	GRCh38
NC_000001.10:g.92732007A>G , CM000663.1:g.92732007A>G	GRCh37
NC_000001.9:g.92504595A>G	NCBI36
NG_009796.1:g.37560T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1183T>C MANE Select	ENSP00000359385.3:p.Leu395=
ENST00000370360.7:c.1183T>C	ENSP00000359385.3:p.Leu395=
ENST00000463560.1:c.562+90T>C
ENST00000495106.5:c.1183T>C	ENSP00000436829.1:p.Leu395=
ENST00000495852.6:c.406T>C	ENSP00000469157.2:p.Leu136=
NM_053274.2:c.1183T>C	NP_444504.1:p.Leu395=
XM_005270400.1:c.1141T>C	XP_005270457.1:p.Leu381=
XM_005270401.2:c.1057T>C	XP_005270458.1:p.Leu353=
XM_006710309.1:c.682T>C	XP_006710372.1:p.Leu228=
XM_011540544.1:c.1183T>C	XP_011538846.1:p.Leu395=
XM_011540545.1:c.1183T>C	XP_011538847.1:p.Leu395=
XM_011540546.1:c.1183T>C	XP_011538848.1:p.Leu395=
XR_946529.1:n.1309+90T>C
NM_001319683.1:c.1141T>C	NP_001306612.1:p.Leu381=
NR_135089.1:n.1298T>C
XM_005270401.3:c.1057T>C	XP_005270458.1:p.Leu353=
XM_006710309.2:c.682T>C	XP_006710372.1:p.Leu228=
XM_011540546.2:c.1183T>C	XP_011538848.1:p.Leu395=
XM_017000137.1:c.1282T>C	XP_016855626.1:p.Leu428=
XM_017000138.1:c.1240T>C	XP_016855627.1:p.Leu414=
XM_017000139.1:c.1293+90T>C	XP_016855628.1:n.1293+90T>C
XM_017000140.1:c.1156T>C	XP_016855629.1:p.Leu386=
XM_017000141.1:c.1194+90T>C	XP_016855630.1:n.1194+90T>C
XM_017000142.1:c.640T>C	XP_016855631.1:p.Leu214=
XM_017000143.1:c.640T>C	XP_016855632.1:p.Leu214=
XM_017000144.1:c.412T>C	XP_016855633.1:p.Leu138=
XR_002959248.1:n.1677+90T>C
XR_002959249.1:n.1309+90T>C
NM_053274.3:c.1183T>C MANE Select	NP_444504.1:p.Leu395=
NM_001319683.2:c.1141T>C	NP_001306612.1:p.Leu381=
NR_135089.2:n.1276T>C