Canonical Allele Identifier: CA1180698869

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266448C= , CM000663.2:g.92266448C=	GRCh38
NC_000001.10:g.92732005C= , CM000663.1:g.92732005C=	GRCh37
NC_000001.9:g.92504593C=	NCBI36
NG_009796.1:g.37562G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1185G= MANE Select	ENSP00000359385.3:p.Leu395=
ENST00000370360.7:c.1185G=	ENSP00000359385.3:p.Leu395=
ENST00000463560.1:c.562+92G=
ENST00000495106.5:c.1185G=	ENSP00000436829.1:p.Leu395=
ENST00000495852.6:c.408G=	ENSP00000469157.2:p.Leu136=
NM_053274.2:c.1185G=	NP_444504.1:p.Leu395=
XM_005270400.1:c.1143G=	XP_005270457.1:p.Leu381=
XM_005270401.2:c.1059G=	XP_005270458.1:p.Leu353=
XM_006710309.1:c.684G=	XP_006710372.1:p.Leu228=
XM_011540544.1:c.1185G=	XP_011538846.1:p.Leu395=
XM_011540545.1:c.1185G=	XP_011538847.1:p.Leu395=
XM_011540546.1:c.1185G=	XP_011538848.1:p.Leu395=
XR_946529.1:n.1309+92G=
NM_001319683.1:c.1143G=	NP_001306612.1:p.Leu381=
NR_135089.1:n.1300G=
XM_005270401.3:c.1059G=	XP_005270458.1:p.Leu353=
XM_006710309.2:c.684G=	XP_006710372.1:p.Leu228=
XM_011540546.2:c.1185G=	XP_011538848.1:p.Leu395=
XM_017000137.1:c.1284G=	XP_016855626.1:p.Leu428=
XM_017000138.1:c.1242G=	XP_016855627.1:p.Leu414=
XM_017000139.1:c.1293+92G=	XP_016855628.1:n.1293+92G=
XM_017000140.1:c.1158G=	XP_016855629.1:p.Leu386=
XM_017000141.1:c.1194+92G=	XP_016855630.1:n.1194+92G=
XM_017000142.1:c.642G=	XP_016855631.1:p.Leu214=
XM_017000143.1:c.642G=	XP_016855632.1:p.Leu214=
XM_017000144.1:c.414G=	XP_016855633.1:p.Leu138=
XR_002959248.1:n.1677+92G=
XR_002959249.1:n.1309+92G=
NM_053274.3:c.1185G= MANE Select	NP_444504.1:p.Leu395=
NM_001319683.2:c.1143G=	NP_001306612.1:p.Leu381=
NR_135089.2:n.1278G=