Canonical Allele Identifier: CA4034142

Gene: UTRN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.144730458G>A , CM000668.2:g.144730458G>A	GRCh38
NC_000006.11:g.145051594G>A , CM000668.1:g.145051594G>A	GRCh37
NC_000006.10:g.145093287G>A	NCBI36
NG_042293.1:g.443722G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_007124.3:c.7911G>A MANE Select	NP_009055.2:p.Glu2637=
ENST00000367545.8:c.7911G>A MANE Select	ENSP00000356515.3:p.Glu2637=
NM_001375323.1:c.576G>A	NP_001362252.1:p.Glu192=
NM_007124.2:c.7911G>A	NP_009055.2:p.Glu2637=
ENST00000367524.8:c.576G>A	ENSP00000356494.4:p.Glu192=
ENST00000367526.8:c.576G>A	ENSP00000356496.4:p.Glu192=
ENST00000367545.7:c.7911G>A	ENSP00000356515.3:p.Glu2637=
XM_005267127.3:c.7926G>A	XP_005267184.1:p.Glu2642=
XM_005267127.5:c.7926G>A	XP_005267184.1:p.Glu2642=
XM_005267130.1:c.7911G>A	XP_005267187.1:p.Glu2637=
XM_005267130.2:c.7911G>A	XP_005267187.1:p.Glu2637=
XM_005267133.1:c.7884G>A	XP_005267190.1:p.Glu2628=
XM_005267133.3:c.7884G>A	XP_005267190.1:p.Glu2628=
XM_006715560.2:c.483G>A	XP_006715623.1:p.Glu161=
XM_006715560.4:c.483G>A	XP_006715623.1:p.Glu161=
XM_011536101.1:c.8019G>A	XP_011534403.1:p.Glu2673=
XM_011536101.3:c.8019G>A	XP_011534403.1:p.Glu2673=
XM_011536102.1:c.8019G>A	XP_011534404.1:p.Glu2673=
XM_011536102.2:c.8019G>A	XP_011534404.1:p.Glu2673=
XM_011536103.1:c.8019G>A	XP_011534405.1:p.Glu2673=
XM_011536104.1:c.8016G>A	XP_011534406.1:p.Glu2672=
XM_011536105.1:c.8019G>A	XP_011534407.1:p.Glu2673=
XM_011536106.1:c.7911G>A	XP_011534408.1:p.Glu2637=
XM_011536106.2:c.7911G>A	XP_011534408.1:p.Glu2637=
XM_011536107.1:c.7884G>A	XP_011534409.1:p.Glu2628=
XM_011536109.1:c.576G>A	XP_011534411.1:p.Glu192=
XM_011536109.3:c.576G>A	XP_011534411.1:p.Glu192=
XM_017011243.2:c.8016G>A	XP_016866732.1:p.Glu2672=
XM_017011244.1:c.8019G>A	XP_016866733.1:p.Glu2673=
XM_024446536.1:c.7884G>A	XP_024302304.1:p.Glu2628=