Canonical Allele Identifier: CA1866632280

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675524T= , CM000671.2:g.97675524T=	GRCh38
NC_000009.11:g.100437806T= , CM000671.1:g.100437806T=	GRCh37
NC_000009.10:g.99477627T=	NCBI36
NG_011642.1:g.26886A= , LRG_471:g.26886A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.737A= MANE Select	ENSP00000364270.5:p.Tyr246=
ENST00000375128.4:c.737A=	ENSP00000364270.4:p.Tyr246=
ENST00000462523.5:c.*173A=	ENSP00000433006.1:n.*173A=
ENST00000485042.1:n.249A=
NM_000380.3:c.737A= , LRG_471t1:c.737A=	NP_000371.1:p.Tyr246=
NR_027302.1:n.1085A=
XM_006717278.1:c.737A=	XP_006717341.1:p.Tyr246=
XM_011518988.1:c.737A=	XP_011517290.1:p.Tyr246=
XR_929839.1:n.1268A=
NM_001354975.1:c.611A=	NP_001341904.1:p.Tyr204=
NR_149091.1:n.582A=
NR_149092.1:n.748A=
NR_149093.1:n.1274A=
NR_149094.1:n.1168A=
NM_000380.4:c.737A= MANE Select	NP_000371.1:p.Tyr246=
NM_001354975.2:c.611A=	NP_001341904.1:p.Tyr204=
NR_027302.2:n.1016A=
NR_149091.2:n.513A=
NR_149092.2:n.679A=
NR_149093.2:n.1205A=
NR_149094.2:n.1099A=