Canonical Allele Identifier: CA418785852

Gene: GLMN

Linked Data

• gnomAD v4: 1-92266436-G-A
• MyVariant Identifiers: chr1:g.92731993G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266436G>A , CM000663.2:g.92266436G>A	GRCh38
NC_000001.10:g.92731993G>A , CM000663.1:g.92731993G>A	GRCh37
NC_000001.9:g.92504581G>A	NCBI36
NG_009796.1:g.37574C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1197C>T MANE Select	ENSP00000359385.3:p.Gly399=
ENST00000370360.7:c.1197C>T	ENSP00000359385.3:p.Gly399=
ENST00000463560.1:c.562+104C>T
ENST00000495106.5:c.1197C>T	ENSP00000436829.1:p.Gly399=
ENST00000495852.6:c.420C>T	ENSP00000469157.2:p.Gly140=
NM_053274.2:c.1197C>T	NP_444504.1:p.Gly399=
XM_005270400.1:c.1155C>T	XP_005270457.1:p.Gly385=
XM_005270401.2:c.1071C>T	XP_005270458.1:p.Gly357=
XM_006710309.1:c.696C>T	XP_006710372.1:p.Gly232=
XM_011540544.1:c.1197C>T	XP_011538846.1:p.Gly399=
XM_011540545.1:c.1197C>T	XP_011538847.1:p.Gly399=
XM_011540546.1:c.1197C>T	XP_011538848.1:p.Gly399=
XR_946529.1:n.1309+104C>T
NM_001319683.1:c.1155C>T	NP_001306612.1:p.Gly385=
NR_135089.1:n.1312C>T
XM_005270401.3:c.1071C>T	XP_005270458.1:p.Gly357=
XM_006710309.2:c.696C>T	XP_006710372.1:p.Gly232=
XM_011540546.2:c.1197C>T	XP_011538848.1:p.Gly399=
XM_017000137.1:c.1296C>T	XP_016855626.1:p.Gly432=
XM_017000138.1:c.1254C>T	XP_016855627.1:p.Gly418=
XM_017000139.1:c.1293+104C>T	XP_016855628.1:n.1293+104C>T
XM_017000140.1:c.1170C>T	XP_016855629.1:p.Gly390=
XM_017000141.1:c.1194+104C>T	XP_016855630.1:n.1194+104C>T
XM_017000142.1:c.654C>T	XP_016855631.1:p.Gly218=
XM_017000143.1:c.654C>T	XP_016855632.1:p.Gly218=
XM_017000144.1:c.426C>T	XP_016855633.1:p.Gly142=
XR_002959248.1:n.1677+104C>T
XR_002959249.1:n.1309+104C>T
NM_053274.3:c.1197C>T MANE Select	NP_444504.1:p.Gly399=
NM_001319683.2:c.1155C>T	NP_001306612.1:p.Gly385=
NR_135089.2:n.1290C>T