Canonical Allele Identifier: CA341099678

Gene: GLMN

Linked Data

• gnomAD v4: 1-92266455-T-C
• MyVariant Identifiers: chr1:g.92732012T>C (hg19) ; chr1:g.92266455T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266455T>C , CM000663.2:g.92266455T>C	GRCh38
NC_000001.10:g.92732012T>C , CM000663.1:g.92732012T>C	GRCh37
NC_000001.9:g.92504600T>C	NCBI36
NG_009796.1:g.37555A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1178A>G MANE Select	ENSP00000359385.3:p.Asn393Ser
ENST00000370360.7:c.1178A>G	ENSP00000359385.3:p.Asn393Ser
ENST00000463560.1:c.562+85A>G
ENST00000495106.5:c.1178A>G	ENSP00000436829.1:p.Asn393Ser
ENST00000495852.6:c.401A>G	ENSP00000469157.2:p.Asn134Ser
NM_053274.2:c.1178A>G	NP_444504.1:p.Asn393Ser
XM_005270400.1:c.1136A>G	XP_005270457.1:p.Asn379Ser
XM_005270401.2:c.1052A>G	XP_005270458.1:p.Asn351Ser
XM_006710309.1:c.677A>G	XP_006710372.1:p.Asn226Ser
XM_011540544.1:c.1178A>G	XP_011538846.1:p.Asn393Ser
XM_011540545.1:c.1178A>G	XP_011538847.1:p.Asn393Ser
XM_011540546.1:c.1178A>G	XP_011538848.1:p.Asn393Ser
XR_946529.1:n.1309+85A>G
NM_001319683.1:c.1136A>G	NP_001306612.1:p.Asn379Ser
NR_135089.1:n.1293A>G
XM_005270401.3:c.1052A>G	XP_005270458.1:p.Asn351Ser
XM_006710309.2:c.677A>G	XP_006710372.1:p.Asn226Ser
XM_011540546.2:c.1178A>G	XP_011538848.1:p.Asn393Ser
XM_017000137.1:c.1277A>G	XP_016855626.1:p.Asn426Ser
XM_017000138.1:c.1235A>G	XP_016855627.1:p.Asn412Ser
XM_017000139.1:c.1293+85A>G	XP_016855628.1:n.1293+85A>G
XM_017000140.1:c.1151A>G	XP_016855629.1:p.Asn384Ser
XM_017000141.1:c.1194+85A>G	XP_016855630.1:n.1194+85A>G
XM_017000142.1:c.635A>G	XP_016855631.1:p.Asn212Ser
XM_017000143.1:c.635A>G	XP_016855632.1:p.Asn212Ser
XM_017000144.1:c.407A>G	XP_016855633.1:p.Asn136Ser
XR_002959248.1:n.1677+85A>G
XR_002959249.1:n.1309+85A>G
NM_053274.3:c.1178A>G MANE Select	NP_444504.1:p.Asn393Ser
NM_001319683.2:c.1136A>G	NP_001306612.1:p.Asn379Ser
NR_135089.2:n.1271A>G