Canonical Allele Identifier: CA740357008

Gene: GLMN

Linked Data

• dbSNP Id: rs1244024374
• MyVariant Identifiers: chr1:g.92731761_92731764del (hg19) ; chr1:g.92266204_92266207del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266204_92266207del , CM000663.2:g.92266204_92266207del	GRCh38
NC_000001.10:g.92731761_92731764del , CM000663.1:g.92731761_92731764del	GRCh37
NC_000001.9:g.92504349_92504352del	NCBI36
NG_009796.1:g.37803_37806del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+212_1214+215del MANE Select	ENSP00000359385.3:n.1214+212_1214+215del
ENST00000370360.7:c.1214+212_1214+215del	ENSP00000359385.3:n.1214+212_1214+215del
ENST00000463560.1:c.562+333_562+336del
ENST00000495106.5:c.1214+212_1214+215del	ENSP00000436829.1:n.1214+212_1214+215del
ENST00000495852.6:c.437+212_437+215del	ENSP00000469157.2:n.437+212_437+215del
NM_053274.2:c.1214+212_1214+215del	NP_444504.1:n.1214+212_1214+215del
XM_005270400.1:c.1172+212_1172+215del	XP_005270457.1:n.1172+212_1172+215del
XM_005270401.2:c.1088+212_1088+215del	XP_005270458.1:n.1088+212_1088+215del
XM_006710309.1:c.713+212_713+215del	XP_006710372.1:n.713+212_713+215del
XM_011540544.1:c.1214+212_1214+215del	XP_011538846.1:n.1214+212_1214+215del
XM_011540545.1:c.1214+212_1214+215del	XP_011538847.1:n.1214+212_1214+215del
XM_011540546.1:c.1214+212_1214+215del	XP_011538848.1:n.1214+212_1214+215del
XR_946529.1:n.1309+333_1309+336del
NM_001319683.1:c.1172+212_1172+215del	NP_001306612.1:n.1172+212_1172+215del
NR_135089.1:n.1329+212_1329+215del
XM_005270401.3:c.1088+212_1088+215del	XP_005270458.1:n.1088+212_1088+215del
XM_006710309.2:c.713+212_713+215del	XP_006710372.1:n.713+212_713+215del
XM_011540546.2:c.1214+212_1214+215del	XP_011538848.1:n.1214+212_1214+215del
XM_017000137.1:c.1313+212_1313+215del	XP_016855626.1:n.1313+212_1313+215del
XM_017000138.1:c.1271+212_1271+215del	XP_016855627.1:n.1271+212_1271+215del
XM_017000139.1:c.1293+333_1293+336del	XP_016855628.1:n.1293+333_1293+336del
XM_017000140.1:c.1187+212_1187+215del	XP_016855629.1:n.1187+212_1187+215del
XM_017000141.1:c.1194+333_1194+336del	XP_016855630.1:n.1194+333_1194+336del
XM_017000142.1:c.671+212_671+215del	XP_016855631.1:n.671+212_671+215del
XM_017000143.1:c.671+212_671+215del	XP_016855632.1:n.671+212_671+215del
XM_017000144.1:c.443+212_443+215del	XP_016855633.1:n.443+212_443+215del
XR_002959248.1:n.1677+333_1677+336del
XR_002959249.1:n.1309+333_1309+336del
NM_053274.3:c.1214+212_1214+215del MANE Select	NP_444504.1:n.1214+212_1214+215del
NM_001319683.2:c.1172+212_1172+215del	NP_001306612.1:n.1172+212_1172+215del
NR_135089.2:n.1307+212_1307+215del