Canonical Allele Identifier: CA341099684

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92732013T>C (hg19) ; chr1:g.92266456T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266456T>C , CM000663.2:g.92266456T>C	GRCh38
NC_000001.10:g.92732013T>C , CM000663.1:g.92732013T>C	GRCh37
NC_000001.9:g.92504601T>C	NCBI36
NG_009796.1:g.37554A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1177A>G MANE Select	ENSP00000359385.3:p.Asn393Asp
ENST00000370360.7:c.1177A>G	ENSP00000359385.3:p.Asn393Asp
ENST00000463560.1:c.562+84A>G
ENST00000495106.5:c.1177A>G	ENSP00000436829.1:p.Asn393Asp
ENST00000495852.6:c.400A>G	ENSP00000469157.2:p.Asn134Asp
NM_053274.2:c.1177A>G	NP_444504.1:p.Asn393Asp
XM_005270400.1:c.1135A>G	XP_005270457.1:p.Asn379Asp
XM_005270401.2:c.1051A>G	XP_005270458.1:p.Asn351Asp
XM_006710309.1:c.676A>G	XP_006710372.1:p.Asn226Asp
XM_011540544.1:c.1177A>G	XP_011538846.1:p.Asn393Asp
XM_011540545.1:c.1177A>G	XP_011538847.1:p.Asn393Asp
XM_011540546.1:c.1177A>G	XP_011538848.1:p.Asn393Asp
XR_946529.1:n.1309+84A>G
NM_001319683.1:c.1135A>G	NP_001306612.1:p.Asn379Asp
NR_135089.1:n.1292A>G
XM_005270401.3:c.1051A>G	XP_005270458.1:p.Asn351Asp
XM_006710309.2:c.676A>G	XP_006710372.1:p.Asn226Asp
XM_011540546.2:c.1177A>G	XP_011538848.1:p.Asn393Asp
XM_017000137.1:c.1276A>G	XP_016855626.1:p.Asn426Asp
XM_017000138.1:c.1234A>G	XP_016855627.1:p.Asn412Asp
XM_017000139.1:c.1293+84A>G	XP_016855628.1:n.1293+84A>G
XM_017000140.1:c.1150A>G	XP_016855629.1:p.Asn384Asp
XM_017000141.1:c.1194+84A>G	XP_016855630.1:n.1194+84A>G
XM_017000142.1:c.634A>G	XP_016855631.1:p.Asn212Asp
XM_017000143.1:c.634A>G	XP_016855632.1:p.Asn212Asp
XM_017000144.1:c.406A>G	XP_016855633.1:p.Asn136Asp
XR_002959248.1:n.1677+84A>G
XR_002959249.1:n.1309+84A>G
NM_053274.3:c.1177A>G MANE Select	NP_444504.1:p.Asn393Asp
NM_001319683.2:c.1135A>G	NP_001306612.1:p.Asn379Asp
NR_135089.2:n.1270A>G