Canonical Allele Identifier: CA374185368

Gene: XPA

Linked Data

• MyVariant Identifiers: chr9:g.100437779T>A (hg19) ; chr9:g.97675497T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675497T>A , CM000671.2:g.97675497T>A	GRCh38
NC_000009.11:g.100437779T>A , CM000671.1:g.100437779T>A	GRCh37
NC_000009.10:g.99477600T>A	NCBI36
NG_011642.1:g.26913A>T , LRG_471:g.26913A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.764A>T MANE Select	ENSP00000364270.5:p.Asp255Val
ENST00000375128.4:c.764A>T	ENSP00000364270.4:p.Asp255Val
ENST00000462523.5:c.*200A>T	ENSP00000433006.1:n.*200A>T
ENST00000485042.1:n.276A>T
NM_000380.3:c.764A>T , LRG_471t1:c.764A>T	NP_000371.1:p.Asp255Val
NR_027302.1:n.1112A>T
XM_006717278.1:c.764A>T	XP_006717341.1:p.Asp255Val
XM_011518988.1:c.764A>T	XP_011517290.1:p.Asp255Val
XR_929839.1:n.1295A>T
NM_001354975.1:c.638A>T	NP_001341904.1:p.Asp213Val
NR_149091.1:n.609A>T
NR_149092.1:n.775A>T
NR_149093.1:n.1301A>T
NR_149094.1:n.1195A>T
NM_000380.4:c.764A>T MANE Select	NP_000371.1:p.Asp255Val
NM_001354975.2:c.638A>T	NP_001341904.1:p.Asp213Val
NR_027302.2:n.1043A>T
NR_149091.2:n.540A>T
NR_149092.2:n.706A>T
NR_149093.2:n.1232A>T
NR_149094.2:n.1126A>T