Canonical Allele Identifier: CA1180711238

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92297877G= , CM000663.2:g.92297877G=	GRCh38
NC_000001.10:g.92763434G= , CM000663.1:g.92763434G=	GRCh37
NC_000001.9:g.92536022G=	NCBI36
NG_009796.1:g.6133C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370360.8:c.39+84C= MANE Select	ENSP00000359385.3:n.39+84C=
ENST00000370360.7:c.39+84C=	ENSP00000359385.3:n.39+84C=
ENST00000487911.1:n.216C=
ENST00000495106.5:c.39+84C=	ENSP00000436829.1:n.39+84C=
NM_053274.2:c.39+84C=	NP_444504.1:n.39+84C=
XM_005270400.1:c.39+84C=	XP_005270457.1:n.39+84C=
XM_005270401.2:c.39+84C=	XP_005270458.1:n.39+84C=
XM_006710309.1:c.-487+84C=	XP_006710372.1:n.-487+84C=
XM_011540544.1:c.39+84C=	XP_011538846.1:n.39+84C=
XM_011540545.1:c.39+84C=	XP_011538847.1:n.39+84C=
XM_011540546.1:c.39+84C=	XP_011538848.1:n.39+84C=
XR_946529.1:n.154+84C=
NM_001319683.1:c.39+84C=	NP_001306612.1:n.39+84C=
NR_135089.1:n.154+84C=
XM_005270401.3:c.39+84C=	XP_005270458.1:n.39+84C=
XM_006710309.2:c.-487+84C=	XP_006710372.1:n.-487+84C=
XM_011540546.2:c.39+84C=	XP_011538848.1:n.39+84C=
XM_017000137.1:c.138+84C=	XP_016855626.1:n.138+84C=
XM_017000138.1:c.138+84C=	XP_016855627.1:n.138+84C=
XM_017000139.1:c.138+84C=	XP_016855628.1:n.138+84C=
XM_017000140.1:c.138+84C=	XP_016855629.1:n.138+84C=
XM_017000141.1:c.39+84C=	XP_016855630.1:n.39+84C=
XM_017000142.1:c.-487+84C=	XP_016855631.1:n.-487+84C=
XM_017000143.1:c.-487+84C=	XP_016855632.1:n.-487+84C=
XM_017000144.1:c.-654+84C=	XP_016855633.1:n.-654+84C=
XR_002959248.1:n.522+84C=
XR_002959249.1:n.154+84C=
NM_053274.3:c.39+84C= MANE Select	NP_444504.1:n.39+84C=
NM_001319683.2:c.39+84C=	NP_001306612.1:n.39+84C=
NR_135089.2:n.132+84C=