Canonical Allele Identifier: CA1866632261

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675495T= , CM000671.2:g.97675495T=	GRCh38
NC_000009.11:g.100437777T= , CM000671.1:g.100437777T=	GRCh37
NC_000009.10:g.99477598T=	NCBI36
NG_011642.1:g.26915A= , LRG_471:g.26915A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.766A= MANE Select	ENSP00000364270.5:p.Met256=
ENST00000375128.4:c.766A=	ENSP00000364270.4:p.Met256=
ENST00000462523.5:c.*202A=	ENSP00000433006.1:n.*202A=
ENST00000485042.1:n.278A=
NM_000380.3:c.766A= , LRG_471t1:c.766A=	NP_000371.1:p.Met256=
NR_027302.1:n.1114A=
XM_006717278.1:c.766A=	XP_006717341.1:p.Met256=
XM_011518988.1:c.766A=	XP_011517290.1:p.Met256=
NM_001354975.1:c.640A=	NP_001341904.1:p.Met214=
NR_149091.1:n.611A=
NR_149092.1:n.777A=
NR_149093.1:n.1303A=
NR_149094.1:n.1197A=
NM_000380.4:c.766A= MANE Select	NP_000371.1:p.Met256=
NM_001354975.2:c.640A=	NP_001341904.1:p.Met214=
NR_027302.2:n.1045A=
NR_149091.2:n.542A=
NR_149092.2:n.708A=
NR_149093.2:n.1234A=
NR_149094.2:n.1128A=