Canonical Allele Identifier: CA1153587926

Gene: UBIAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11274199A= , CM000663.2:g.11274199A=	GRCh38
NC_000001.10:g.11334256A= , CM000663.1:g.11334256A=	GRCh37
NC_000001.9:g.11256843A=	NCBI36
NG_009443.1:g.6002A=
NG_009443.2:g.6002A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.529+139A= MANE Select	ENSP00000366006.5:n.529+139A=
ENST00000376804.2:c.529+139A=	ENSP00000366000.1:n.529+139A=
ENST00000376810.5:c.529+139A=	ENSP00000366006.5:n.529+139A=
ENST00000483738.1:c.127+139A=	ENSP00000473453.1:n.127+139A=
ENST00000486588.6:c.172+139A=	ENSP00000473612.1:n.172+139A=
NM_013319.2:c.529+139A=	NP_037451.1:n.529+139A=
XM_006710590.2:c.529+139A=	XP_006710653.1:n.529+139A=
XM_011541304.1:c.529+139A=	XP_011539606.1:n.529+139A=
XR_946616.1:n.863+139A=
NM_001330349.1:c.529+139A=	NP_001317278.1:n.529+139A=
NM_001330350.1:c.529+139A=	NP_001317279.1:n.529+139A=
XR_946616.3:n.863+139A=
NM_001330349.2:c.529+139A=	NP_001317278.1:n.529+139A=
NM_001330350.2:c.529+139A=	NP_001317279.1:n.529+139A=
NM_013319.3:c.529+139A= MANE Select	NP_037451.1:n.529+139A=