Canonical Allele Identifier: CA4032546

Gene: UTRN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.144458976C>T , CM000668.2:g.144458976C>T	GRCh38
NC_000006.11:g.144780112C>T , CM000668.1:g.144780112C>T	GRCh37
NC_000006.10:g.144821805C>T	NCBI36
NG_042293.1:g.172240C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367545.8:c.2491C>T MANE Select	ENSP00000356515.3:p.Arg831Trp
ENST00000367545.7:c.2491C>T	ENSP00000356515.3:p.Arg831Trp
NM_007124.2:c.2491C>T	NP_009055.2:p.Arg831Trp
XM_005267127.3:c.2506C>T	XP_005267184.1:p.Arg836Trp
XM_005267130.1:c.2491C>T	XP_005267187.1:p.Arg831Trp
XM_005267133.1:c.2464C>T	XP_005267190.1:p.Arg822Trp
XM_011536101.1:c.2599C>T	XP_011534403.1:p.Arg867Trp
XM_011536102.1:c.2599C>T	XP_011534404.1:p.Arg867Trp
XM_011536103.1:c.2599C>T	XP_011534405.1:p.Arg867Trp
XM_011536104.1:c.2596C>T	XP_011534406.1:p.Arg866Trp
XM_011536105.1:c.2599C>T	XP_011534407.1:p.Arg867Trp
XM_011536106.1:c.2491C>T	XP_011534408.1:p.Arg831Trp
XM_011536107.1:c.2464C>T	XP_011534409.1:p.Arg822Trp
XM_011536108.1:c.2599C>T	XP_011534410.1:p.Arg867Trp
XM_005267127.5:c.2506C>T	XP_005267184.1:p.Arg836Trp
XM_005267130.2:c.2491C>T	XP_005267187.1:p.Arg831Trp
XM_005267133.3:c.2464C>T	XP_005267190.1:p.Arg822Trp
XM_011536101.3:c.2599C>T	XP_011534403.1:p.Arg867Trp
XM_011536102.2:c.2599C>T	XP_011534404.1:p.Arg867Trp
XM_011536106.2:c.2491C>T	XP_011534408.1:p.Arg831Trp
XM_017011243.2:c.2596C>T	XP_016866732.1:p.Arg866Trp
XM_017011244.1:c.2599C>T	XP_016866733.1:p.Arg867Trp
XM_017011245.1:c.2599C>T	XP_016866734.1:p.Arg867Trp
XM_024446536.1:c.2464C>T	XP_024302304.1:p.Arg822Trp
NM_007124.3:c.2491C>T MANE Select	NP_009055.2:p.Arg831Trp