Canonical Allele Identifier: CA1180698875

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266458A= , CM000663.2:g.92266458A=	GRCh38
NC_000001.10:g.92732015A= , CM000663.1:g.92732015A=	GRCh37
NC_000001.9:g.92504603A=	NCBI36
NG_009796.1:g.37552T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1175T= MANE Select	ENSP00000359385.3:p.Ile392=
ENST00000370360.7:c.1175T=	ENSP00000359385.3:p.Ile392=
ENST00000463560.1:c.562+82T=
ENST00000495106.5:c.1175T=	ENSP00000436829.1:p.Ile392=
ENST00000495852.6:c.398T=	ENSP00000469157.2:p.Ile133=
NM_053274.2:c.1175T=	NP_444504.1:p.Ile392=
XM_005270400.1:c.1133T=	XP_005270457.1:p.Ile378=
XM_005270401.2:c.1049T=	XP_005270458.1:p.Ile350=
XM_006710309.1:c.674T=	XP_006710372.1:p.Ile225=
XM_011540544.1:c.1175T=	XP_011538846.1:p.Ile392=
XM_011540545.1:c.1175T=	XP_011538847.1:p.Ile392=
XM_011540546.1:c.1175T=	XP_011538848.1:p.Ile392=
XR_946529.1:n.1309+82T=
NM_001319683.1:c.1133T=	NP_001306612.1:p.Ile378=
NR_135089.1:n.1290T=
XM_005270401.3:c.1049T=	XP_005270458.1:p.Ile350=
XM_006710309.2:c.674T=	XP_006710372.1:p.Ile225=
XM_011540546.2:c.1175T=	XP_011538848.1:p.Ile392=
XM_017000137.1:c.1274T=	XP_016855626.1:p.Ile425=
XM_017000138.1:c.1232T=	XP_016855627.1:p.Ile411=
XM_017000139.1:c.1293+82T=	XP_016855628.1:n.1293+82T=
XM_017000140.1:c.1148T=	XP_016855629.1:p.Ile383=
XM_017000141.1:c.1194+82T=	XP_016855630.1:n.1194+82T=
XM_017000142.1:c.632T=	XP_016855631.1:p.Ile211=
XM_017000143.1:c.632T=	XP_016855632.1:p.Ile211=
XM_017000144.1:c.404T=	XP_016855633.1:p.Ile135=
XR_002959248.1:n.1677+82T=
XR_002959249.1:n.1309+82T=
NM_053274.3:c.1175T= MANE Select	NP_444504.1:p.Ile392=
NM_001319683.2:c.1133T=	NP_001306612.1:p.Ile378=
NR_135089.2:n.1268T=