Canonical Allele Identifier: CA365932244

Gene: UTRN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.144491023G>T , CM000668.2:g.144491023G>T	GRCh38
NC_000006.11:g.144812159G>T , CM000668.1:g.144812159G>T	GRCh37
NC_000006.10:g.144853852G>T	NCBI36
NG_042293.1:g.204287G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007124.3:c.4358G>T MANE Select	NP_009055.2:p.Gly1453Val
ENST00000367545.8:c.4358G>T MANE Select	ENSP00000356515.3:p.Gly1453Val
NM_007124.2:c.4358G>T	NP_009055.2:p.Gly1453Val
ENST00000367545.7:c.4358G>T	ENSP00000356515.3:p.Gly1453Val
XM_005267127.3:c.4373G>T	XP_005267184.1:p.Gly1458Val
XM_005267127.5:c.4373G>T	XP_005267184.1:p.Gly1458Val
XM_005267130.1:c.4358G>T	XP_005267187.1:p.Gly1453Val
XM_005267130.2:c.4358G>T	XP_005267187.1:p.Gly1453Val
XM_005267133.1:c.4331G>T	XP_005267190.1:p.Gly1444Val
XM_005267133.3:c.4331G>T	XP_005267190.1:p.Gly1444Val
XM_011536101.1:c.4466G>T	XP_011534403.1:p.Gly1489Val
XM_011536101.3:c.4466G>T	XP_011534403.1:p.Gly1489Val
XM_011536102.1:c.4466G>T	XP_011534404.1:p.Gly1489Val
XM_011536102.2:c.4466G>T	XP_011534404.1:p.Gly1489Val
XM_011536103.1:c.4466G>T	XP_011534405.1:p.Gly1489Val
XM_011536104.1:c.4463G>T	XP_011534406.1:p.Gly1488Val
XM_011536105.1:c.4466G>T	XP_011534407.1:p.Gly1489Val
XM_011536106.1:c.4358G>T	XP_011534408.1:p.Gly1453Val
XM_011536106.2:c.4358G>T	XP_011534408.1:p.Gly1453Val
XM_011536107.1:c.4331G>T	XP_011534409.1:p.Gly1444Val
XM_011536108.1:c.4466G>T	XP_011534410.1:p.Gly1489Val
XM_017011243.2:c.4463G>T	XP_016866732.1:p.Gly1488Val
XM_017011244.1:c.4466G>T	XP_016866733.1:p.Gly1489Val
XM_017011245.1:c.4466G>T	XP_016866734.1:p.Gly1489Val
XM_024446536.1:c.4331G>T	XP_024302304.1:p.Gly1444Val