Canonical Allele Identifier: CA1866632281

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675527T= , CM000671.2:g.97675527T=	GRCh38
NC_000009.11:g.100437809T= , CM000671.1:g.100437809T=	GRCh37
NC_000009.10:g.99477630T=	NCBI36
NG_011642.1:g.26883A= , LRG_471:g.26883A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.734A= MANE Select	ENSP00000364270.5:p.Glu245=
ENST00000375128.4:c.734A=	ENSP00000364270.4:p.Glu245=
ENST00000462523.5:c.*170A=	ENSP00000433006.1:n.*170A=
ENST00000485042.1:n.246A=
NM_000380.3:c.734A= , LRG_471t1:c.734A=	NP_000371.1:p.Glu245=
NR_027302.1:n.1082A=
XM_006717278.1:c.734A=	XP_006717341.1:p.Glu245=
XM_011518988.1:c.734A=	XP_011517290.1:p.Glu245=
XR_929839.1:n.1265A=
NM_001354975.1:c.608A=	NP_001341904.1:p.Glu203=
NR_149091.1:n.579A=
NR_149092.1:n.745A=
NR_149093.1:n.1271A=
NR_149094.1:n.1165A=
NM_000380.4:c.734A= MANE Select	NP_000371.1:p.Glu245=
NM_001354975.2:c.608A=	NP_001341904.1:p.Glu203=
NR_027302.2:n.1013A=
NR_149091.2:n.510A=
NR_149092.2:n.676A=
NR_149093.2:n.1202A=
NR_149094.2:n.1096A=