Canonical Allele Identifier: CA1866632451

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675804T= , CM000671.2:g.97675804T=	GRCh38
NC_000009.11:g.100438086T= , CM000671.1:g.100438086T=	GRCh37
NC_000009.10:g.99477907T=	NCBI36
NG_011642.1:g.26606A= , LRG_471:g.26606A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-217A= MANE Select	ENSP00000364270.5:n.674-217A=
ENST00000375128.4:c.674-217A=	ENSP00000364270.4:n.674-217A=
ENST00000462523.5:c.*110-217A=	ENSP00000433006.1:n.*110-217A=
ENST00000485042.1:n.152A=
NM_000380.3:c.674-217A= , LRG_471t1:c.674-217A=	NP_000371.1:n.674-217A=
NR_027302.1:n.1022-217A=
XM_006717278.1:c.674-217A=	XP_006717341.1:n.674-217A=
XM_011518988.1:c.674-217A=	XP_011517290.1:n.674-217A=
XR_929839.1:n.1171A=
NM_001354975.1:c.548-217A=	NP_001341904.1:n.548-217A=
NR_149091.1:n.519-217A=
NR_149092.1:n.685-217A=
NR_149093.1:n.1177A=
NR_149094.1:n.1071A=
NM_000380.4:c.674-217A= MANE Select	NP_000371.1:n.674-217A=
NM_001354975.2:c.548-217A=	NP_001341904.1:n.548-217A=
NR_027302.2:n.953-217A=
NR_149091.2:n.450-217A=
NR_149092.2:n.616-217A=
NR_149093.2:n.1108A=
NR_149094.2:n.1002A=