Canonical Allele Identifier: CA950342

Gene: GLMN

Linked Data

• dbSNP Id: rs779986327
• ExAC: 1:92732084 GAATA / G
• gnomAD v2: 1-92732084-GAATA-G
• gnomAD v4: 1-92266527-GAATA-G
• MyVariant Identifiers: chr1:g.92732085_92732088del (hg19) ; chr1:g.92266528_92266531del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266530_92266533del , CM000663.2:g.92266530_92266533del	GRCh38
NC_000001.10:g.92732087_92732090del , CM000663.1:g.92732087_92732090del	GRCh37
NC_000001.9:g.92504675_92504678del	NCBI36
NG_009796.1:g.37479_37482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1141-39_1141-36del MANE Select	ENSP00000359385.3:n.1141-39_1141-36del
ENST00000370360.7:c.1141-39_1141-36del	ENSP00000359385.3:n.1141-39_1141-36del
ENST00000463560.1:c.562+9_562+12del
ENST00000495106.5:c.1141-39_1141-36del	ENSP00000436829.1:n.1141-39_1141-36del
ENST00000495852.6:c.364-39_364-36del	ENSP00000469157.2:n.364-39_364-36del
NM_053274.2:c.1141-39_1141-36del	NP_444504.1:n.1141-39_1141-36del
XM_005270400.1:c.1099-39_1099-36del	XP_005270457.1:n.1099-39_1099-36del
XM_005270401.2:c.1015-39_1015-36del	XP_005270458.1:n.1015-39_1015-36del
XM_006710309.1:c.640-39_640-36del	XP_006710372.1:n.640-39_640-36del
XM_011540544.1:c.1141-39_1141-36del	XP_011538846.1:n.1141-39_1141-36del
XM_011540545.1:c.1141-39_1141-36del	XP_011538847.1:n.1141-39_1141-36del
XM_011540546.1:c.1141-39_1141-36del	XP_011538848.1:n.1141-39_1141-36del
XR_946529.1:n.1309+9_1309+12del
NM_001319683.1:c.1099-39_1099-36del	NP_001306612.1:n.1099-39_1099-36del
NR_135089.1:n.1256-39_1256-36del
XM_005270401.3:c.1015-39_1015-36del	XP_005270458.1:n.1015-39_1015-36del
XM_006710309.2:c.640-39_640-36del	XP_006710372.1:n.640-39_640-36del
XM_011540546.2:c.1141-39_1141-36del	XP_011538848.1:n.1141-39_1141-36del
XM_017000137.1:c.1240-39_1240-36del	XP_016855626.1:n.1240-39_1240-36del
XM_017000138.1:c.1198-39_1198-36del	XP_016855627.1:n.1198-39_1198-36del
XM_017000139.1:c.1293+9_1293+12del	XP_016855628.1:n.1293+9_1293+12del
XM_017000140.1:c.1114-39_1114-36del	XP_016855629.1:n.1114-39_1114-36del
XM_017000141.1:c.1194+9_1194+12del	XP_016855630.1:n.1194+9_1194+12del
XM_017000142.1:c.598-39_598-36del	XP_016855631.1:n.598-39_598-36del
XM_017000143.1:c.598-39_598-36del	XP_016855632.1:n.598-39_598-36del
XM_017000144.1:c.370-39_370-36del	XP_016855633.1:n.370-39_370-36del
XR_002959248.1:n.1677+9_1677+12del
XR_002959249.1:n.1309+9_1309+12del
NM_053274.3:c.1141-39_1141-36del MANE Select	NP_444504.1:n.1141-39_1141-36del
NM_001319683.2:c.1099-39_1099-36del	NP_001306612.1:n.1099-39_1099-36del
NR_135089.2:n.1234-39_1234-36del