Canonical Allele Identifier: CA1866632470

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675854A= , CM000671.2:g.97675854A=	GRCh38
NC_000009.11:g.100438136A= , CM000671.1:g.100438136A=	GRCh37
NC_000009.10:g.99477957A=	NCBI36
NG_011642.1:g.26556T= , LRG_471:g.26556T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-267T= MANE Select	ENSP00000364270.5:n.674-267T=
ENST00000375128.4:c.674-267T=	ENSP00000364270.4:n.674-267T=
ENST00000462523.5:c.*110-267T=	ENSP00000433006.1:n.*110-267T=
ENST00000485042.1:n.102T=
NM_000380.3:c.674-267T= , LRG_471t1:c.674-267T=	NP_000371.1:n.674-267T=
NR_027302.1:n.1022-267T=
XM_006717278.1:c.674-267T=	XP_006717341.1:n.674-267T=
XM_011518988.1:c.674-267T=	XP_011517290.1:n.674-267T=
XR_929839.1:n.1121T=
NM_001354975.1:c.548-267T=	NP_001341904.1:n.548-267T=
NR_149091.1:n.519-267T=
NR_149092.1:n.685-267T=
NR_149093.1:n.1127T=
NR_149094.1:n.1021T=
NM_000380.4:c.674-267T= MANE Select	NP_000371.1:n.674-267T=
NM_001354975.2:c.548-267T=	NP_001341904.1:n.548-267T=
NR_027302.2:n.953-267T=
NR_149091.2:n.450-267T=
NR_149092.2:n.616-267T=
NR_149093.2:n.1058T=
NR_149094.2:n.952T=