Canonical Allele Identifier: CA1866632283

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675530T= , CM000671.2:g.97675530T=	GRCh38
NC_000009.11:g.100437812T= , CM000671.1:g.100437812T=	GRCh37
NC_000009.10:g.99477633T=	NCBI36
NG_011642.1:g.26880A= , LRG_471:g.26880A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.731A= MANE Select	ENSP00000364270.5:p.His244=
ENST00000375128.4:c.731A=	ENSP00000364270.4:p.His244=
ENST00000462523.5:c.*167A=	ENSP00000433006.1:n.*167A=
ENST00000485042.1:n.243A=
NM_000380.3:c.731A= , LRG_471t1:c.731A=	NP_000371.1:p.His244=
NR_027302.1:n.1079A=
XM_006717278.1:c.731A=	XP_006717341.1:p.His244=
XM_011518988.1:c.731A=	XP_011517290.1:p.His244=
XR_929839.1:n.1262A=
NM_001354975.1:c.605A=	NP_001341904.1:p.His202=
NR_149091.1:n.576A=
NR_149092.1:n.742A=
NR_149093.1:n.1268A=
NR_149094.1:n.1162A=
NM_000380.4:c.731A= MANE Select	NP_000371.1:p.His244=
NM_001354975.2:c.605A=	NP_001341904.1:p.His202=
NR_027302.2:n.1010A=
NR_149091.2:n.507A=
NR_149092.2:n.673A=
NR_149093.2:n.1199A=
NR_149094.2:n.1093A=