Canonical Allele Identifier: CA1180698960

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266624_92266625delinsTA , CM000663.2:g.92266624_92266625delinsTA	GRCh38
NC_000001.10:g.92732181_92732182delinsTA , CM000663.1:g.92732181_92732182delinsTA	GRCh37
NC_000001.9:g.92504769_92504770delinsTA	NCBI36
NG_009796.1:g.37385_37386delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1140+75_1140+76delinsTA MANE Select	ENSP00000359385.3:n.1140+75_1140+76delinsTA
ENST00000370360.7:c.1140+75_1140+76delinsTA	ENSP00000359385.3:n.1140+75_1140+76delinsTA
ENST00000463560.1:c.509-32_509-31delinsTA
ENST00000495106.5:c.1140+75_1140+76delinsTA	ENSP00000436829.1:n.1140+75_1140+76delinsTA
ENST00000495852.6:c.364-133_364-132delinsTA	ENSP00000469157.2:n.364-133_364-132delinsTA
NM_053274.2:c.1140+75_1140+76delinsTA	NP_444504.1:n.1140+75_1140+76delinsTA
XM_005270400.1:c.1099-133_1099-132delinsTA	XP_005270457.1:n.1099-133_1099-132delinsTA
XM_005270401.2:c.1014+75_1014+76delinsTA	XP_005270458.1:n.1014+75_1014+76delinsTA
XM_006710309.1:c.639+75_639+76delinsTA	XP_006710372.1:n.639+75_639+76delinsTA
XM_011540544.1:c.1140+75_1140+76delinsTA	XP_011538846.1:n.1140+75_1140+76delinsTA
XM_011540545.1:c.1140+75_1140+76delinsTA	XP_011538847.1:n.1140+75_1140+76delinsTA
XM_011540546.1:c.1140+75_1140+76delinsTA	XP_011538848.1:n.1140+75_1140+76delinsTA
XR_946529.1:n.1256-32_1256-31delinsTA
NM_001319683.1:c.1099-133_1099-132delinsTA	NP_001306612.1:n.1099-133_1099-132delinsTA
NR_135089.1:n.1255+75_1255+76delinsTA
XM_005270401.3:c.1014+75_1014+76delinsTA	XP_005270458.1:n.1014+75_1014+76delinsTA
XM_006710309.2:c.639+75_639+76delinsTA	XP_006710372.1:n.639+75_639+76delinsTA
XM_011540546.2:c.1140+75_1140+76delinsTA	XP_011538848.1:n.1140+75_1140+76delinsTA
XM_017000137.1:c.1239+75_1239+76delinsTA	XP_016855626.1:n.1239+75_1239+76delinsTA
XM_017000138.1:c.1198-133_1198-132delinsTA	XP_016855627.1:n.1198-133_1198-132delinsTA
XM_017000139.1:c.1240-32_1240-31delinsTA	XP_016855628.1:n.1240-32_1240-31delinsTA
XM_017000140.1:c.1113+75_1113+76delinsTA	XP_016855629.1:n.1113+75_1113+76delinsTA
XM_017000141.1:c.1141-32_1141-31delinsTA	XP_016855630.1:n.1141-32_1141-31delinsTA
XM_017000142.1:c.598-133_598-132delinsTA	XP_016855631.1:n.598-133_598-132delinsTA
XM_017000143.1:c.598-133_598-132delinsTA	XP_016855632.1:n.598-133_598-132delinsTA
XM_017000144.1:c.369+75_369+76delinsTA	XP_016855633.1:n.369+75_369+76delinsTA
XR_002959248.1:n.1624-32_1624-31delinsTA
XR_002959249.1:n.1256-32_1256-31delinsTA
NM_053274.3:c.1140+75_1140+76delinsTA MANE Select	NP_444504.1:n.1140+75_1140+76delinsTA
NM_001319683.2:c.1099-133_1099-132delinsTA	NP_001306612.1:n.1099-133_1099-132delinsTA
NR_135089.2:n.1233+75_1233+76delinsTA