Canonical Allele Identifier: CA1180698982

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266660C= , CM000663.2:g.92266660C=	GRCh38
NC_000001.10:g.92732217C= , CM000663.1:g.92732217C=	GRCh37
NC_000001.9:g.92504805C=	NCBI36
NG_009796.1:g.37350G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1140+40G= MANE Select	ENSP00000359385.3:n.1140+40G=
ENST00000370360.7:c.1140+40G=	ENSP00000359385.3:n.1140+40G=
ENST00000463560.1:c.508+40G=
ENST00000495106.5:c.1140+40G=	ENSP00000436829.1:n.1140+40G=
ENST00000495852.6:c.364-168G=	ENSP00000469157.2:n.364-168G=
NM_053274.2:c.1140+40G=	NP_444504.1:n.1140+40G=
XM_005270400.1:c.1099-168G=	XP_005270457.1:n.1099-168G=
XM_005270401.2:c.1014+40G=	XP_005270458.1:n.1014+40G=
XM_006710309.1:c.639+40G=	XP_006710372.1:n.639+40G=
XM_011540544.1:c.1140+40G=	XP_011538846.1:n.1140+40G=
XM_011540545.1:c.1140+40G=	XP_011538847.1:n.1140+40G=
XM_011540546.1:c.1140+40G=	XP_011538848.1:n.1140+40G=
XR_946529.1:n.1255+40G=
NM_001319683.1:c.1099-168G=	NP_001306612.1:n.1099-168G=
NR_135089.1:n.1255+40G=
XM_005270401.3:c.1014+40G=	XP_005270458.1:n.1014+40G=
XM_006710309.2:c.639+40G=	XP_006710372.1:n.639+40G=
XM_011540546.2:c.1140+40G=	XP_011538848.1:n.1140+40G=
XM_017000137.1:c.1239+40G=	XP_016855626.1:n.1239+40G=
XM_017000138.1:c.1198-168G=	XP_016855627.1:n.1198-168G=
XM_017000139.1:c.1239+40G=	XP_016855628.1:n.1239+40G=
XM_017000140.1:c.1113+40G=	XP_016855629.1:n.1113+40G=
XM_017000141.1:c.1140+40G=	XP_016855630.1:n.1140+40G=
XM_017000142.1:c.598-168G=	XP_016855631.1:n.598-168G=
XM_017000143.1:c.598-168G=	XP_016855632.1:n.598-168G=
XM_017000144.1:c.369+40G=	XP_016855633.1:n.369+40G=
XR_002959248.1:n.1623+40G=
XR_002959249.1:n.1255+40G=
NM_053274.3:c.1140+40G= MANE Select	NP_444504.1:n.1140+40G=
NM_001319683.2:c.1099-168G=	NP_001306612.1:n.1099-168G=
NR_135089.2:n.1233+40G=