Canonical Allele Identifier: CA374185484

Gene: XPA

Linked Data

• MyVariant Identifiers: chr9:g.100437830T>G (hg19) ; chr9:g.97675548T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675548T>G , CM000671.2:g.97675548T>G	GRCh38
NC_000009.11:g.100437830T>G , CM000671.1:g.100437830T>G	GRCh37
NC_000009.10:g.99477651T>G	NCBI36
NG_011642.1:g.26862A>C , LRG_471:g.26862A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.713A>C MANE Select	ENSP00000364270.5:p.Glu238Ala
ENST00000375128.4:c.713A>C	ENSP00000364270.4:p.Glu238Ala
ENST00000462523.5:c.*149A>C	ENSP00000433006.1:n.*149A>C
ENST00000485042.1:n.225A>C
NM_000380.3:c.713A>C , LRG_471t1:c.713A>C	NP_000371.1:p.Glu238Ala
NR_027302.1:n.1061A>C
XM_006717278.1:c.713A>C	XP_006717341.1:p.Glu238Ala
XM_011518988.1:c.713A>C	XP_011517290.1:p.Glu238Ala
XR_929839.1:n.1244A>C
NM_001354975.1:c.587A>C	NP_001341904.1:p.Glu196Ala
NR_149091.1:n.558A>C
NR_149092.1:n.724A>C
NR_149093.1:n.1250A>C
NR_149094.1:n.1144A>C
NM_000380.4:c.713A>C MANE Select	NP_000371.1:p.Glu238Ala
NM_001354975.2:c.587A>C	NP_001341904.1:p.Glu196Ala
NR_027302.2:n.992A>C
NR_149091.2:n.489A>C
NR_149092.2:n.655A>C
NR_149093.2:n.1181A>C
NR_149094.2:n.1075A>C