Canonical Allele Identifier: CA1866632211

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675396T= , CM000671.2:g.97675396T=	GRCh38
NC_000009.11:g.100437678T= , CM000671.1:g.100437678T=	GRCh37
NC_000009.10:g.99477499T=	NCBI36
NG_011642.1:g.27014A= , LRG_471:g.27014A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.*43A= MANE Select	ENSP00000364270.5:n.*43A=
ENST00000375128.4:c.*43A=	ENSP00000364270.4:n.*43A=
ENST00000462523.5:c.*301A=	ENSP00000433006.1:n.*301A=
ENST00000485042.1:n.377A=
NM_000380.3:c.*43A= , LRG_471t1:c.*43A=	NP_000371.1:n.*43A=
NR_027302.1:n.1213A=
XM_006717278.1:c.772+93A=	XP_006717341.1:n.772+93A=
XM_011518988.1:c.772+93A=	XP_011517290.1:n.772+93A=
NM_001354975.1:c.*43A=	NP_001341904.1:n.*43A=
NR_149091.1:n.710A=
NR_149092.1:n.876A=
NR_149093.1:n.1402A=
NR_149094.1:n.1296A=
NM_000380.4:c.*43A= MANE Select	NP_000371.1:n.*43A=
NM_001354975.2:c.*43A=	NP_001341904.1:n.*43A=
NR_027302.2:n.1144A=
NR_149091.2:n.641A=
NR_149092.2:n.807A=
NR_149093.2:n.1333A=
NR_149094.2:n.1227A=