Canonical Allele Identifier: CA341099630

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92732003T>A (hg19) ; chr1:g.92266446T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266446T>A , CM000663.2:g.92266446T>A	GRCh38
NC_000001.10:g.92732003T>A , CM000663.1:g.92732003T>A	GRCh37
NC_000001.9:g.92504591T>A	NCBI36
NG_009796.1:g.37564A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1187A>T MANE Select	ENSP00000359385.3:p.Asp396Val
ENST00000370360.7:c.1187A>T	ENSP00000359385.3:p.Asp396Val
ENST00000463560.1:c.562+94A>T
ENST00000495106.5:c.1187A>T	ENSP00000436829.1:p.Asp396Val
ENST00000495852.6:c.410A>T	ENSP00000469157.2:p.Asp137Val
NM_053274.2:c.1187A>T	NP_444504.1:p.Asp396Val
XM_005270400.1:c.1145A>T	XP_005270457.1:p.Asp382Val
XM_005270401.2:c.1061A>T	XP_005270458.1:p.Asp354Val
XM_006710309.1:c.686A>T	XP_006710372.1:p.Asp229Val
XM_011540544.1:c.1187A>T	XP_011538846.1:p.Asp396Val
XM_011540545.1:c.1187A>T	XP_011538847.1:p.Asp396Val
XM_011540546.1:c.1187A>T	XP_011538848.1:p.Asp396Val
XR_946529.1:n.1309+94A>T
NM_001319683.1:c.1145A>T	NP_001306612.1:p.Asp382Val
NR_135089.1:n.1302A>T
XM_005270401.3:c.1061A>T	XP_005270458.1:p.Asp354Val
XM_006710309.2:c.686A>T	XP_006710372.1:p.Asp229Val
XM_011540546.2:c.1187A>T	XP_011538848.1:p.Asp396Val
XM_017000137.1:c.1286A>T	XP_016855626.1:p.Asp429Val
XM_017000138.1:c.1244A>T	XP_016855627.1:p.Asp415Val
XM_017000139.1:c.1293+94A>T	XP_016855628.1:n.1293+94A>T
XM_017000140.1:c.1160A>T	XP_016855629.1:p.Asp387Val
XM_017000141.1:c.1194+94A>T	XP_016855630.1:n.1194+94A>T
XM_017000142.1:c.644A>T	XP_016855631.1:p.Asp215Val
XM_017000143.1:c.644A>T	XP_016855632.1:p.Asp215Val
XM_017000144.1:c.416A>T	XP_016855633.1:p.Asp139Val
XR_002959248.1:n.1677+94A>T
XR_002959249.1:n.1309+94A>T
NM_053274.3:c.1187A>T MANE Select	NP_444504.1:p.Asp396Val
NM_001319683.2:c.1145A>T	NP_001306612.1:p.Asp382Val
NR_135089.2:n.1280A>T