Canonical Allele Identifier: CA341099707

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92732018T>G (hg19) ; chr1:g.92266461T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266461T>G , CM000663.2:g.92266461T>G	GRCh38
NC_000001.10:g.92732018T>G , CM000663.1:g.92732018T>G	GRCh37
NC_000001.9:g.92504606T>G	NCBI36
NG_009796.1:g.37549A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1172A>C MANE Select	ENSP00000359385.3:p.Tyr391Ser
ENST00000370360.7:c.1172A>C	ENSP00000359385.3:p.Tyr391Ser
ENST00000463560.1:c.562+79A>C
ENST00000495106.5:c.1172A>C	ENSP00000436829.1:p.Tyr391Ser
ENST00000495852.6:c.395A>C	ENSP00000469157.2:p.Tyr132Ser
NM_053274.2:c.1172A>C	NP_444504.1:p.Tyr391Ser
XM_005270400.1:c.1130A>C	XP_005270457.1:p.Tyr377Ser
XM_005270401.2:c.1046A>C	XP_005270458.1:p.Tyr349Ser
XM_006710309.1:c.671A>C	XP_006710372.1:p.Tyr224Ser
XM_011540544.1:c.1172A>C	XP_011538846.1:p.Tyr391Ser
XM_011540545.1:c.1172A>C	XP_011538847.1:p.Tyr391Ser
XM_011540546.1:c.1172A>C	XP_011538848.1:p.Tyr391Ser
XR_946529.1:n.1309+79A>C
NM_001319683.1:c.1130A>C	NP_001306612.1:p.Tyr377Ser
NR_135089.1:n.1287A>C
XM_005270401.3:c.1046A>C	XP_005270458.1:p.Tyr349Ser
XM_006710309.2:c.671A>C	XP_006710372.1:p.Tyr224Ser
XM_011540546.2:c.1172A>C	XP_011538848.1:p.Tyr391Ser
XM_017000137.1:c.1271A>C	XP_016855626.1:p.Tyr424Ser
XM_017000138.1:c.1229A>C	XP_016855627.1:p.Tyr410Ser
XM_017000139.1:c.1293+79A>C	XP_016855628.1:n.1293+79A>C
XM_017000140.1:c.1145A>C	XP_016855629.1:p.Tyr382Ser
XM_017000141.1:c.1194+79A>C	XP_016855630.1:n.1194+79A>C
XM_017000142.1:c.629A>C	XP_016855631.1:p.Tyr210Ser
XM_017000143.1:c.629A>C	XP_016855632.1:p.Tyr210Ser
XM_017000144.1:c.401A>C	XP_016855633.1:p.Tyr134Ser
XR_002959248.1:n.1677+79A>C
XR_002959249.1:n.1309+79A>C
NM_053274.3:c.1172A>C MANE Select	NP_444504.1:p.Tyr391Ser
NM_001319683.2:c.1130A>C	NP_001306612.1:p.Tyr377Ser
NR_135089.2:n.1265A>C