Canonical Allele Identifier: CA2427841091

Gene: UBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47193872C= , CM000685.2:g.47193872C=	GRCh38
NC_000023.10:g.47053271C= , CM000685.1:g.47053271C=	GRCh37
NC_000023.9:g.46938215C=	NCBI36
NG_009161.1:g.8073C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000335972.11:c.-153C= MANE Select	ENSP00000338413.6:n.-153C=
ENST00000335972.10:c.-153C=	ENSP00000338413.6:n.-153C=
ENST00000377351.8:c.-1+2922C=	ENSP00000366568.4:n.-1+2922C=
ENST00000412206.5:c.-1+2138C=	ENSP00000415033.1:n.-1+2138C=
ENST00000427561.5:c.-6+2305C=	ENSP00000397816.1:n.-6+2305C=
ENST00000442035.5:c.-158C=	ENSP00000389583.1:n.-158C=
ENST00000457753.5:c.-189C=	ENSP00000404796.1:n.-189C=
NM_003334.3:c.-153C=	NP_003325.2:n.-153C=
NM_153280.2:c.-1+2922C=	NP_695012.1:n.-1+2922C=
XM_005272649.1:c.-213C=	XP_005272706.1:n.-213C=
XM_005272650.1:c.-267C=	XP_005272707.1:n.-267C=
XM_011543953.1:c.-230C=	XP_011542255.1:n.-230C=
XM_011543954.1:c.-158C=	XP_011542256.1:n.-158C=
XM_011543955.1:c.-210C=	XP_011542257.1:n.-210C=
XM_011543954.2:c.-158C=	XP_011542256.1:n.-158C=
NM_003334.4:c.-153C= MANE Select	NP_003325.2:n.-153C=
NM_153280.3:c.-1+2922C=	NP_695012.1:n.-1+2922C=