Canonical Allele Identifier: CA1866632441

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675786T= , CM000671.2:g.97675786T=	GRCh38
NC_000009.11:g.100438068T= , CM000671.1:g.100438068T=	GRCh37
NC_000009.10:g.99477889T=	NCBI36
NG_011642.1:g.26624A= , LRG_471:g.26624A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-199A= MANE Select	ENSP00000364270.5:n.674-199A=
ENST00000375128.4:c.674-199A=	ENSP00000364270.4:n.674-199A=
ENST00000462523.5:c.*110-199A=	ENSP00000433006.1:n.*110-199A=
ENST00000485042.1:n.170A=
NM_000380.3:c.674-199A= , LRG_471t1:c.674-199A=	NP_000371.1:n.674-199A=
NR_027302.1:n.1022-199A=
XM_006717278.1:c.674-199A=	XP_006717341.1:n.674-199A=
XM_011518988.1:c.674-199A=	XP_011517290.1:n.674-199A=
XR_929839.1:n.1189A=
NM_001354975.1:c.548-199A=	NP_001341904.1:n.548-199A=
NR_149091.1:n.519-199A=
NR_149092.1:n.685-199A=
NR_149093.1:n.1195A=
NR_149094.1:n.1089A=
NM_000380.4:c.674-199A= MANE Select	NP_000371.1:n.674-199A=
NM_001354975.2:c.548-199A=	NP_001341904.1:n.548-199A=
NR_027302.2:n.953-199A=
NR_149091.2:n.450-199A=
NR_149092.2:n.616-199A=
NR_149093.2:n.1126A=
NR_149094.2:n.1020A=