Canonical Allele Identifier: CA1180698914

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266530_92266532delinsTAA , CM000663.2:g.92266530_92266532delinsTAA	GRCh38
NC_000001.10:g.92732087_92732089delinsTAA , CM000663.1:g.92732087_92732089delinsTAA	GRCh37
NC_000001.9:g.92504675_92504677delinsTAA	NCBI36
NG_009796.1:g.37478_37480delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1141-40_1141-38delinsTTA MANE Select	ENSP00000359385.3:n.1141-40_1141-38delinsTTA
ENST00000370360.7:c.1141-40_1141-38delinsTTA	ENSP00000359385.3:n.1141-40_1141-38delinsTTA
ENST00000463560.1:c.562+8_562+10delinsTTA
ENST00000495106.5:c.1141-40_1141-38delinsTTA	ENSP00000436829.1:n.1141-40_1141-38delinsTTA
ENST00000495852.6:c.364-40_364-38delinsTTA	ENSP00000469157.2:n.364-40_364-38delinsTTA
NM_053274.2:c.1141-40_1141-38delinsTTA	NP_444504.1:n.1141-40_1141-38delinsTTA
XM_005270400.1:c.1099-40_1099-38delinsTTA	XP_005270457.1:n.1099-40_1099-38delinsTTA
XM_005270401.2:c.1015-40_1015-38delinsTTA	XP_005270458.1:n.1015-40_1015-38delinsTTA
XM_006710309.1:c.640-40_640-38delinsTTA	XP_006710372.1:n.640-40_640-38delinsTTA
XM_011540544.1:c.1141-40_1141-38delinsTTA	XP_011538846.1:n.1141-40_1141-38delinsTTA
XM_011540545.1:c.1141-40_1141-38delinsTTA	XP_011538847.1:n.1141-40_1141-38delinsTTA
XM_011540546.1:c.1141-40_1141-38delinsTTA	XP_011538848.1:n.1141-40_1141-38delinsTTA
XR_946529.1:n.1309+8_1309+10delinsTTA
NM_001319683.1:c.1099-40_1099-38delinsTTA	NP_001306612.1:n.1099-40_1099-38delinsTTA
NR_135089.1:n.1256-40_1256-38delinsTTA
XM_005270401.3:c.1015-40_1015-38delinsTTA	XP_005270458.1:n.1015-40_1015-38delinsTTA
XM_006710309.2:c.640-40_640-38delinsTTA	XP_006710372.1:n.640-40_640-38delinsTTA
XM_011540546.2:c.1141-40_1141-38delinsTTA	XP_011538848.1:n.1141-40_1141-38delinsTTA
XM_017000137.1:c.1240-40_1240-38delinsTTA	XP_016855626.1:n.1240-40_1240-38delinsTTA
XM_017000138.1:c.1198-40_1198-38delinsTTA	XP_016855627.1:n.1198-40_1198-38delinsTTA
XM_017000139.1:c.1293+8_1293+10delinsTTA	XP_016855628.1:n.1293+8_1293+10delinsTTA
XM_017000140.1:c.1114-40_1114-38delinsTTA	XP_016855629.1:n.1114-40_1114-38delinsTTA
XM_017000141.1:c.1194+8_1194+10delinsTTA	XP_016855630.1:n.1194+8_1194+10delinsTTA
XM_017000142.1:c.598-40_598-38delinsTTA	XP_016855631.1:n.598-40_598-38delinsTTA
XM_017000143.1:c.598-40_598-38delinsTTA	XP_016855632.1:n.598-40_598-38delinsTTA
XM_017000144.1:c.370-40_370-38delinsTTA	XP_016855633.1:n.370-40_370-38delinsTTA
XR_002959248.1:n.1677+8_1677+10delinsTTA
XR_002959249.1:n.1309+8_1309+10delinsTTA
NM_053274.3:c.1141-40_1141-38delinsTTA MANE Select	NP_444504.1:n.1141-40_1141-38delinsTTA
NM_001319683.2:c.1099-40_1099-38delinsTTA	NP_001306612.1:n.1099-40_1099-38delinsTTA
NR_135089.2:n.1234-40_1234-38delinsTTA