Canonical Allele Identifier: CA418785862

Gene: GLMN

Linked Data

• gnomAD v4: 1-92266454-G-A
• MyVariant Identifiers: chr1:g.92732011G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266454G>A , CM000663.2:g.92266454G>A	GRCh38
NC_000001.10:g.92732011G>A , CM000663.1:g.92732011G>A	GRCh37
NC_000001.9:g.92504599G>A	NCBI36
NG_009796.1:g.37556C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1179C>T MANE Select	ENSP00000359385.3:p.Asn393=
ENST00000370360.7:c.1179C>T	ENSP00000359385.3:p.Asn393=
ENST00000463560.1:c.562+86C>T
ENST00000495106.5:c.1179C>T	ENSP00000436829.1:p.Asn393=
ENST00000495852.6:c.402C>T	ENSP00000469157.2:p.Asn134=
NM_053274.2:c.1179C>T	NP_444504.1:p.Asn393=
XM_005270400.1:c.1137C>T	XP_005270457.1:p.Asn379=
XM_005270401.2:c.1053C>T	XP_005270458.1:p.Asn351=
XM_006710309.1:c.678C>T	XP_006710372.1:p.Asn226=
XM_011540544.1:c.1179C>T	XP_011538846.1:p.Asn393=
XM_011540545.1:c.1179C>T	XP_011538847.1:p.Asn393=
XM_011540546.1:c.1179C>T	XP_011538848.1:p.Asn393=
XR_946529.1:n.1309+86C>T
NM_001319683.1:c.1137C>T	NP_001306612.1:p.Asn379=
NR_135089.1:n.1294C>T
XM_005270401.3:c.1053C>T	XP_005270458.1:p.Asn351=
XM_006710309.2:c.678C>T	XP_006710372.1:p.Asn226=
XM_011540546.2:c.1179C>T	XP_011538848.1:p.Asn393=
XM_017000137.1:c.1278C>T	XP_016855626.1:p.Asn426=
XM_017000138.1:c.1236C>T	XP_016855627.1:p.Asn412=
XM_017000139.1:c.1293+86C>T	XP_016855628.1:n.1293+86C>T
XM_017000140.1:c.1152C>T	XP_016855629.1:p.Asn384=
XM_017000141.1:c.1194+86C>T	XP_016855630.1:n.1194+86C>T
XM_017000142.1:c.636C>T	XP_016855631.1:p.Asn212=
XM_017000143.1:c.636C>T	XP_016855632.1:p.Asn212=
XM_017000144.1:c.408C>T	XP_016855633.1:p.Asn136=
XR_002959248.1:n.1677+86C>T
XR_002959249.1:n.1309+86C>T
NM_053274.3:c.1179C>T MANE Select	NP_444504.1:p.Asn393=
NM_001319683.2:c.1137C>T	NP_001306612.1:p.Asn379=
NR_135089.2:n.1272C>T