Canonical Allele Identifier: CA1866632286

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675536T= , CM000671.2:g.97675536T=	GRCh38
NC_000009.11:g.100437818T= , CM000671.1:g.100437818T=	GRCh37
NC_000009.10:g.99477639T=	NCBI36
NG_011642.1:g.26874A= , LRG_471:g.26874A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.725A= MANE Select	ENSP00000364270.5:p.His242=
ENST00000375128.4:c.725A=	ENSP00000364270.4:p.His242=
ENST00000462523.5:c.*161A=	ENSP00000433006.1:n.*161A=
ENST00000485042.1:n.237A=
NM_000380.3:c.725A= , LRG_471t1:c.725A=	NP_000371.1:p.His242=
NR_027302.1:n.1073A=
XM_006717278.1:c.725A=	XP_006717341.1:p.His242=
XM_011518988.1:c.725A=	XP_011517290.1:p.His242=
XR_929839.1:n.1256A=
NM_001354975.1:c.599A=	NP_001341904.1:p.His200=
NR_149091.1:n.570A=
NR_149092.1:n.736A=
NR_149093.1:n.1262A=
NR_149094.1:n.1156A=
NM_000380.4:c.725A= MANE Select	NP_000371.1:p.His242=
NM_001354975.2:c.599A=	NP_001341904.1:p.His200=
NR_027302.2:n.1004A=
NR_149091.2:n.501A=
NR_149092.2:n.667A=
NR_149093.2:n.1193A=
NR_149094.2:n.1087A=