Canonical Allele Identifier: CA1180698855

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266417A= , CM000663.2:g.92266417A=	GRCh38
NC_000001.10:g.92731974A= , CM000663.1:g.92731974A=	GRCh37
NC_000001.9:g.92504562A=	NCBI36
NG_009796.1:g.37593T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+2T= MANE Select	ENSP00000359385.3:n.1214+2T=
ENST00000370360.7:c.1214+2T=	ENSP00000359385.3:n.1214+2T=
ENST00000463560.1:c.562+123T=
ENST00000495106.5:c.1214+2T=	ENSP00000436829.1:n.1214+2T=
ENST00000495852.6:c.437+2T=	ENSP00000469157.2:n.437+2T=
NM_053274.2:c.1214+2T=	NP_444504.1:n.1214+2T=
XM_005270400.1:c.1172+2T=	XP_005270457.1:n.1172+2T=
XM_005270401.2:c.1088+2T=	XP_005270458.1:n.1088+2T=
XM_006710309.1:c.713+2T=	XP_006710372.1:n.713+2T=
XM_011540544.1:c.1214+2T=	XP_011538846.1:n.1214+2T=
XM_011540545.1:c.1214+2T=	XP_011538847.1:n.1214+2T=
XM_011540546.1:c.1214+2T=	XP_011538848.1:n.1214+2T=
XR_946529.1:n.1309+123T=
NM_001319683.1:c.1172+2T=	NP_001306612.1:n.1172+2T=
NR_135089.1:n.1329+2T=
XM_005270401.3:c.1088+2T=	XP_005270458.1:n.1088+2T=
XM_006710309.2:c.713+2T=	XP_006710372.1:n.713+2T=
XM_011540546.2:c.1214+2T=	XP_011538848.1:n.1214+2T=
XM_017000137.1:c.1313+2T=	XP_016855626.1:n.1313+2T=
XM_017000138.1:c.1271+2T=	XP_016855627.1:n.1271+2T=
XM_017000139.1:c.1293+123T=	XP_016855628.1:n.1293+123T=
XM_017000140.1:c.1187+2T=	XP_016855629.1:n.1187+2T=
XM_017000141.1:c.1194+123T=	XP_016855630.1:n.1194+123T=
XM_017000142.1:c.671+2T=	XP_016855631.1:n.671+2T=
XM_017000143.1:c.671+2T=	XP_016855632.1:n.671+2T=
XM_017000144.1:c.443+2T=	XP_016855633.1:n.443+2T=
XR_002959248.1:n.1677+123T=
XR_002959249.1:n.1309+123T=
NM_053274.3:c.1214+2T= MANE Select	NP_444504.1:n.1214+2T=
NM_001319683.2:c.1172+2T=	NP_001306612.1:n.1172+2T=
NR_135089.2:n.1307+2T=