Canonical Allele Identifier: CA2427845508

Gene: UBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47206010A= , CM000685.2:g.47206010A=	GRCh38
NC_000023.10:g.47065409A= , CM000685.1:g.47065409A=	GRCh37
NC_000023.9:g.46950353A=	NCBI36
NG_009161.1:g.20211A=
NG_021353.1:g.6163A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335972.11:c.1638A= MANE Select	ENSP00000338413.6:p.Thr546=
ENST00000335972.10:c.1638A=	ENSP00000338413.6:p.Thr546=
ENST00000377351.8:c.1638A=	ENSP00000366568.4:p.Thr546=
ENST00000490869.1:n.465-68A=
NM_003334.3:c.1638A=	NP_003325.2:p.Thr546=
NM_153280.2:c.1638A=	NP_695012.1:p.Thr546=
XM_005272649.1:c.1656A=	XP_005272706.1:p.Thr552=
XM_005272650.1:c.1638A=	XP_005272707.1:p.Thr546=
XM_011543953.1:c.1722A=	XP_011542255.1:p.Thr574=
XM_011543954.1:c.1680A=	XP_011542256.1:p.Thr560=
XM_011543955.1:c.1656A=	XP_011542257.1:p.Thr552=
XM_011543956.1:c.1638A=	XP_011542258.1:p.Thr546=
XR_949047.1:n.216-660T=
XM_011543954.2:c.1680A=	XP_011542256.1:p.Thr560=
XM_017029777.1:c.1791A=	XP_016885266.1:p.Thr597=
XM_017029778.2:c.1722A=	XP_016885267.1:p.Thr574=
XM_017029779.2:c.1656A=	XP_016885268.1:p.Thr552=
XM_017029780.1:c.1638A=	XP_016885269.1:p.Thr546=
XM_017029781.1:c.1638A=	XP_016885270.1:p.Thr546=
XR_949047.3:n.284-660T=
NM_003334.4:c.1638A= MANE Select	NP_003325.2:p.Thr546=
NM_153280.3:c.1638A=	NP_695012.1:p.Thr546=