Canonical Allele Identifier: CA466174805

Gene: XPA

Linked Data

• MyVariant Identifiers: chr9:g.100437778G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675496G>A , CM000671.2:g.97675496G>A	GRCh38
NC_000009.11:g.100437778G>A , CM000671.1:g.100437778G>A	GRCh37
NC_000009.10:g.99477599G>A	NCBI36
NG_011642.1:g.26914C>T , LRG_471:g.26914C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.765C>T MANE Select	ENSP00000364270.5:p.Asp255=
ENST00000375128.4:c.765C>T	ENSP00000364270.4:p.Asp255=
ENST00000462523.5:c.*201C>T	ENSP00000433006.1:n.*201C>T
ENST00000485042.1:n.277C>T
NM_000380.3:c.765C>T , LRG_471t1:c.765C>T	NP_000371.1:p.Asp255=
NR_027302.1:n.1113C>T
XM_006717278.1:c.765C>T	XP_006717341.1:p.Asp255=
XM_011518988.1:c.765C>T	XP_011517290.1:p.Asp255=
XR_929839.1:n.1296C>T
NM_001354975.1:c.639C>T	NP_001341904.1:p.Asp213=
NR_149091.1:n.610C>T
NR_149092.1:n.776C>T
NR_149093.1:n.1302C>T
NR_149094.1:n.1196C>T
NM_000380.4:c.765C>T MANE Select	NP_000371.1:p.Asp255=
NM_001354975.2:c.639C>T	NP_001341904.1:p.Asp213=
NR_027302.2:n.1044C>T
NR_149091.2:n.541C>T
NR_149092.2:n.707C>T
NR_149093.2:n.1233C>T
NR_149094.2:n.1127C>T