Canonical Allele Identifier: CA418785849

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92731984T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266427T>G , CM000663.2:g.92266427T>G	GRCh38
NC_000001.10:g.92731984T>G , CM000663.1:g.92731984T>G	GRCh37
NC_000001.9:g.92504572T>G	NCBI36
NG_009796.1:g.37583A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1206A>C MANE Select	ENSP00000359385.3:p.Thr402=
ENST00000370360.7:c.1206A>C	ENSP00000359385.3:p.Thr402=
ENST00000463560.1:c.562+113A>C
ENST00000495106.5:c.1206A>C	ENSP00000436829.1:p.Thr402=
ENST00000495852.6:c.429A>C	ENSP00000469157.2:p.Thr143=
NM_053274.2:c.1206A>C	NP_444504.1:p.Thr402=
XM_005270400.1:c.1164A>C	XP_005270457.1:p.Thr388=
XM_005270401.2:c.1080A>C	XP_005270458.1:p.Thr360=
XM_006710309.1:c.705A>C	XP_006710372.1:p.Thr235=
XM_011540544.1:c.1206A>C	XP_011538846.1:p.Thr402=
XM_011540545.1:c.1206A>C	XP_011538847.1:p.Thr402=
XM_011540546.1:c.1206A>C	XP_011538848.1:p.Thr402=
XR_946529.1:n.1309+113A>C
NM_001319683.1:c.1164A>C	NP_001306612.1:p.Thr388=
NR_135089.1:n.1321A>C
XM_005270401.3:c.1080A>C	XP_005270458.1:p.Thr360=
XM_006710309.2:c.705A>C	XP_006710372.1:p.Thr235=
XM_011540546.2:c.1206A>C	XP_011538848.1:p.Thr402=
XM_017000137.1:c.1305A>C	XP_016855626.1:p.Thr435=
XM_017000138.1:c.1263A>C	XP_016855627.1:p.Thr421=
XM_017000139.1:c.1293+113A>C	XP_016855628.1:n.1293+113A>C
XM_017000140.1:c.1179A>C	XP_016855629.1:p.Thr393=
XM_017000141.1:c.1194+113A>C	XP_016855630.1:n.1194+113A>C
XM_017000142.1:c.663A>C	XP_016855631.1:p.Thr221=
XM_017000143.1:c.663A>C	XP_016855632.1:p.Thr221=
XM_017000144.1:c.435A>C	XP_016855633.1:p.Thr145=
XR_002959248.1:n.1677+113A>C
XR_002959249.1:n.1309+113A>C
NM_053274.3:c.1206A>C MANE Select	NP_444504.1:p.Thr402=
NM_001319683.2:c.1164A>C	NP_001306612.1:p.Thr388=
NR_135089.2:n.1299A>C