Canonical Allele Identifier: CA338691144

Gene: UBIAD1

Linked Data

• MyVariant Identifiers: chr1:g.11333854T>C (hg19) ; chr1:g.11273797T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11273797T>C , CM000663.2:g.11273797T>C	GRCh38
NC_000001.10:g.11333854T>C , CM000663.1:g.11333854T>C	GRCh37
NC_000001.9:g.11256441T>C	NCBI36
NG_009443.1:g.5600T>C
NG_009443.2:g.5600T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.266T>C MANE Select	ENSP00000366006.5:p.Val89Ala
ENST00000376804.2:c.266T>C	ENSP00000366000.1:p.Val89Ala
ENST00000376810.5:c.266T>C	ENSP00000366006.5:p.Val89Ala
NM_013319.2:c.266T>C	NP_037451.1:p.Val89Ala
XM_006710590.2:c.266T>C	XP_006710653.1:p.Val89Ala
XM_011541304.1:c.266T>C	XP_011539606.1:p.Val89Ala
XR_946616.1:n.600T>C
NM_001330349.1:c.266T>C	NP_001317278.1:p.Val89Ala
NM_001330350.1:c.266T>C	NP_001317279.1:p.Val89Ala
XR_946616.3:n.600T>C
NM_001330349.2:c.266T>C	NP_001317278.1:p.Val89Ala
NM_001330350.2:c.266T>C	NP_001317279.1:p.Val89Ala
NM_013319.3:c.266T>C MANE Select	NP_037451.1:p.Val89Ala