Canonical Allele Identifier: CA2574433020

Gene: GLMN

Linked Data

• gnomAD v4: 1-92297883-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92297883C>T , CM000663.2:g.92297883C>T	GRCh38
NC_000001.10:g.92763440C>T , CM000663.1:g.92763440C>T	GRCh37
NC_000001.9:g.92536028C>T	NCBI36
NG_009796.1:g.6127G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370360.8:c.39+78G>A MANE Select	ENSP00000359385.3:n.39+78G>A
ENST00000370360.7:c.39+78G>A	ENSP00000359385.3:n.39+78G>A
ENST00000487911.1:n.210G>A
ENST00000495106.5:c.39+78G>A	ENSP00000436829.1:n.39+78G>A
NM_053274.2:c.39+78G>A	NP_444504.1:n.39+78G>A
XM_005270400.1:c.39+78G>A	XP_005270457.1:n.39+78G>A
XM_005270401.2:c.39+78G>A	XP_005270458.1:n.39+78G>A
XM_006710309.1:c.-487+78G>A	XP_006710372.1:n.-487+78G>A
XM_011540544.1:c.39+78G>A	XP_011538846.1:n.39+78G>A
XM_011540545.1:c.39+78G>A	XP_011538847.1:n.39+78G>A
XM_011540546.1:c.39+78G>A	XP_011538848.1:n.39+78G>A
XR_946529.1:n.154+78G>A
NM_001319683.1:c.39+78G>A	NP_001306612.1:n.39+78G>A
NR_135089.1:n.154+78G>A
XM_005270401.3:c.39+78G>A	XP_005270458.1:n.39+78G>A
XM_006710309.2:c.-487+78G>A	XP_006710372.1:n.-487+78G>A
XM_011540546.2:c.39+78G>A	XP_011538848.1:n.39+78G>A
XM_017000137.1:c.138+78G>A	XP_016855626.1:n.138+78G>A
XM_017000138.1:c.138+78G>A	XP_016855627.1:n.138+78G>A
XM_017000139.1:c.138+78G>A	XP_016855628.1:n.138+78G>A
XM_017000140.1:c.138+78G>A	XP_016855629.1:n.138+78G>A
XM_017000141.1:c.39+78G>A	XP_016855630.1:n.39+78G>A
XM_017000142.1:c.-487+78G>A	XP_016855631.1:n.-487+78G>A
XM_017000143.1:c.-487+78G>A	XP_016855632.1:n.-487+78G>A
XM_017000144.1:c.-654+78G>A	XP_016855633.1:n.-654+78G>A
XR_002959248.1:n.522+78G>A
XR_002959249.1:n.154+78G>A
NM_053274.3:c.39+78G>A MANE Select	NP_444504.1:n.39+78G>A
NM_001319683.2:c.39+78G>A	NP_001306612.1:n.39+78G>A
NR_135089.2:n.132+78G>A