Canonical Allele Identifier: CA341099541

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92731983A>C (hg19) ; chr1:g.92266426A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266426A>C , CM000663.2:g.92266426A>C	GRCh38
NC_000001.10:g.92731983A>C , CM000663.1:g.92731983A>C	GRCh37
NC_000001.9:g.92504571A>C	NCBI36
NG_009796.1:g.37584T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1207T>G MANE Select	ENSP00000359385.3:p.Leu403Val
ENST00000370360.7:c.1207T>G	ENSP00000359385.3:p.Leu403Val
ENST00000463560.1:c.562+114T>G
ENST00000495106.5:c.1207T>G	ENSP00000436829.1:p.Leu403Val
ENST00000495852.6:c.430T>G	ENSP00000469157.2:p.Leu144Val
NM_053274.2:c.1207T>G	NP_444504.1:p.Leu403Val
XM_005270400.1:c.1165T>G	XP_005270457.1:p.Leu389Val
XM_005270401.2:c.1081T>G	XP_005270458.1:p.Leu361Val
XM_006710309.1:c.706T>G	XP_006710372.1:p.Leu236Val
XM_011540544.1:c.1207T>G	XP_011538846.1:p.Leu403Val
XM_011540545.1:c.1207T>G	XP_011538847.1:p.Leu403Val
XM_011540546.1:c.1207T>G	XP_011538848.1:p.Leu403Val
XR_946529.1:n.1309+114T>G
NM_001319683.1:c.1165T>G	NP_001306612.1:p.Leu389Val
NR_135089.1:n.1322T>G
XM_005270401.3:c.1081T>G	XP_005270458.1:p.Leu361Val
XM_006710309.2:c.706T>G	XP_006710372.1:p.Leu236Val
XM_011540546.2:c.1207T>G	XP_011538848.1:p.Leu403Val
XM_017000137.1:c.1306T>G	XP_016855626.1:p.Leu436Val
XM_017000138.1:c.1264T>G	XP_016855627.1:p.Leu422Val
XM_017000139.1:c.1293+114T>G	XP_016855628.1:n.1293+114T>G
XM_017000140.1:c.1180T>G	XP_016855629.1:p.Leu394Val
XM_017000141.1:c.1194+114T>G	XP_016855630.1:n.1194+114T>G
XM_017000142.1:c.664T>G	XP_016855631.1:p.Leu222Val
XM_017000143.1:c.664T>G	XP_016855632.1:p.Leu222Val
XM_017000144.1:c.436T>G	XP_016855633.1:p.Leu146Val
XR_002959248.1:n.1677+114T>G
XR_002959249.1:n.1309+114T>G
NM_053274.3:c.1207T>G MANE Select	NP_444504.1:p.Leu403Val
NM_001319683.2:c.1165T>G	NP_001306612.1:p.Leu389Val
NR_135089.2:n.1300T>G