Canonical Allele Identifier: CA646102454

Gene: GLMN

Linked Data

• COSMIC: COSN14456469

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266543G>C , CM000663.2:g.92266543G>C	GRCh38
NC_000001.10:g.92732100G>C , CM000663.1:g.92732100G>C	GRCh37
NC_000001.9:g.92504688G>C	NCBI36
NG_009796.1:g.37467C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1141-51C>G MANE Select	ENSP00000359385.3:n.1141-51C>G
ENST00000370360.7:c.1141-51C>G	ENSP00000359385.3:n.1141-51C>G
ENST00000463560.1:c.559C>G
ENST00000495106.5:c.1141-51C>G	ENSP00000436829.1:n.1141-51C>G
ENST00000495852.6:c.364-51C>G	ENSP00000469157.2:n.364-51C>G
NM_053274.2:c.1141-51C>G	NP_444504.1:n.1141-51C>G
XM_005270400.1:c.1099-51C>G	XP_005270457.1:n.1099-51C>G
XM_005270401.2:c.1015-51C>G	XP_005270458.1:n.1015-51C>G
XM_006710309.1:c.640-51C>G	XP_006710372.1:n.640-51C>G
XM_011540544.1:c.1141-51C>G	XP_011538846.1:n.1141-51C>G
XM_011540545.1:c.1141-51C>G	XP_011538847.1:n.1141-51C>G
XM_011540546.1:c.1141-51C>G	XP_011538848.1:n.1141-51C>G
XR_946529.1:n.1306C>G
NM_001319683.1:c.1099-51C>G	NP_001306612.1:n.1099-51C>G
NR_135089.1:n.1256-51C>G
XM_005270401.3:c.1015-51C>G	XP_005270458.1:n.1015-51C>G
XM_006710309.2:c.640-51C>G	XP_006710372.1:n.640-51C>G
XM_011540546.2:c.1141-51C>G	XP_011538848.1:n.1141-51C>G
XM_017000137.1:c.1240-51C>G	XP_016855626.1:n.1240-51C>G
XM_017000138.1:c.1198-51C>G	XP_016855627.1:n.1198-51C>G
XM_017000139.1:c.1290C>G	XP_016855628.1:p.Val430=
XM_017000140.1:c.1114-51C>G	XP_016855629.1:n.1114-51C>G
XM_017000141.1:c.1191C>G	XP_016855630.1:p.Val397=
XM_017000142.1:c.598-51C>G	XP_016855631.1:n.598-51C>G
XM_017000143.1:c.598-51C>G	XP_016855632.1:n.598-51C>G
XM_017000144.1:c.370-51C>G	XP_016855633.1:n.370-51C>G
XR_002959248.1:n.1674C>G
XR_002959249.1:n.1306C>G
NM_053274.3:c.1141-51C>G MANE Select	NP_444504.1:n.1141-51C>G
NM_001319683.2:c.1099-51C>G	NP_001306612.1:n.1099-51C>G
NR_135089.2:n.1234-51C>G