Canonical Allele Identifier: CA1180698865

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266437C= , CM000663.2:g.92266437C=	GRCh38
NC_000001.10:g.92731994C= , CM000663.1:g.92731994C=	GRCh37
NC_000001.9:g.92504582C=	NCBI36
NG_009796.1:g.37573G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1196G= MANE Select	ENSP00000359385.3:p.Gly399=
ENST00000370360.7:c.1196G=	ENSP00000359385.3:p.Gly399=
ENST00000463560.1:c.562+103G=
ENST00000495106.5:c.1196G=	ENSP00000436829.1:p.Gly399=
ENST00000495852.6:c.419G=	ENSP00000469157.2:p.Gly140=
NM_053274.2:c.1196G=	NP_444504.1:p.Gly399=
XM_005270400.1:c.1154G=	XP_005270457.1:p.Gly385=
XM_005270401.2:c.1070G=	XP_005270458.1:p.Gly357=
XM_006710309.1:c.695G=	XP_006710372.1:p.Gly232=
XM_011540544.1:c.1196G=	XP_011538846.1:p.Gly399=
XM_011540545.1:c.1196G=	XP_011538847.1:p.Gly399=
XM_011540546.1:c.1196G=	XP_011538848.1:p.Gly399=
XR_946529.1:n.1309+103G=
NM_001319683.1:c.1154G=	NP_001306612.1:p.Gly385=
NR_135089.1:n.1311G=
XM_005270401.3:c.1070G=	XP_005270458.1:p.Gly357=
XM_006710309.2:c.695G=	XP_006710372.1:p.Gly232=
XM_011540546.2:c.1196G=	XP_011538848.1:p.Gly399=
XM_017000137.1:c.1295G=	XP_016855626.1:p.Gly432=
XM_017000138.1:c.1253G=	XP_016855627.1:p.Gly418=
XM_017000139.1:c.1293+103G=	XP_016855628.1:n.1293+103G=
XM_017000140.1:c.1169G=	XP_016855629.1:p.Gly390=
XM_017000141.1:c.1194+103G=	XP_016855630.1:n.1194+103G=
XM_017000142.1:c.653G=	XP_016855631.1:p.Gly218=
XM_017000143.1:c.653G=	XP_016855632.1:p.Gly218=
XM_017000144.1:c.425G=	XP_016855633.1:p.Gly142=
XR_002959248.1:n.1677+103G=
XR_002959249.1:n.1309+103G=
NM_053274.3:c.1196G= MANE Select	NP_444504.1:p.Gly399=
NM_001319683.2:c.1154G=	NP_001306612.1:p.Gly385=
NR_135089.2:n.1289G=