Canonical Allele Identifier: CA1866632236

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675443A= , CM000671.2:g.97675443A=	GRCh38
NC_000009.11:g.100437725A= , CM000671.1:g.100437725A=	GRCh37
NC_000009.10:g.99477546A=	NCBI36
NG_011642.1:g.26967T= , LRG_471:g.26967T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.818T= MANE Select	ENSP00000364270.5:p.Met273=
ENST00000375128.4:c.818T=	ENSP00000364270.4:p.Met273=
ENST00000462523.5:c.*254T=	ENSP00000433006.1:n.*254T=
ENST00000485042.1:n.330T=
NM_000380.3:c.818T= , LRG_471t1:c.818T=	NP_000371.1:p.Met273=
NR_027302.1:n.1166T=
XM_006717278.1:c.772+46T=	XP_006717341.1:n.772+46T=
XM_011518988.1:c.772+46T=	XP_011517290.1:n.772+46T=
NM_001354975.1:c.692T=	NP_001341904.1:p.Met231=
NR_149091.1:n.663T=
NR_149092.1:n.829T=
NR_149093.1:n.1355T=
NR_149094.1:n.1249T=
NM_000380.4:c.818T= MANE Select	NP_000371.1:p.Met273=
NM_001354975.2:c.692T=	NP_001341904.1:p.Met231=
NR_027302.2:n.1097T=
NR_149091.2:n.594T=
NR_149092.2:n.760T=
NR_149093.2:n.1286T=
NR_149094.2:n.1180T=