Canonical Allele Identifier: CA1866632298

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675562G= , CM000671.2:g.97675562G=	GRCh38
NC_000009.11:g.100437844G= , CM000671.1:g.100437844G=	GRCh37
NC_000009.10:g.99477665G=	NCBI36
NG_011642.1:g.26848C= , LRG_471:g.26848C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.699C= MANE Select	ENSP00000364270.5:p.Ser233=
ENST00000375128.4:c.699C=	ENSP00000364270.4:p.Ser233=
ENST00000462523.5:c.*135C=	ENSP00000433006.1:n.*135C=
ENST00000485042.1:n.211C=
NM_000380.3:c.699C= , LRG_471t1:c.699C=	NP_000371.1:p.Ser233=
NR_027302.1:n.1047C=
XM_006717278.1:c.699C=	XP_006717341.1:p.Ser233=
XM_011518988.1:c.699C=	XP_011517290.1:p.Ser233=
XR_929839.1:n.1230C=
NM_001354975.1:c.573C=	NP_001341904.1:p.Ser191=
NR_149091.1:n.544C=
NR_149092.1:n.710C=
NR_149093.1:n.1236C=
NR_149094.1:n.1130C=
NM_000380.4:c.699C= MANE Select	NP_000371.1:p.Ser233=
NM_001354975.2:c.573C=	NP_001341904.1:p.Ser191=
NR_027302.2:n.978C=
NR_149091.2:n.475C=
NR_149092.2:n.641C=
NR_149093.2:n.1167C=
NR_149094.2:n.1061C=