Canonical Allele Identifier: CA1866632262

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675499A= , CM000671.2:g.97675499A=	GRCh38
NC_000009.11:g.100437781A= , CM000671.1:g.100437781A=	GRCh37
NC_000009.10:g.99477602A=	NCBI36
NG_011642.1:g.26911T= , LRG_471:g.26911T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.762T= MANE Select	ENSP00000364270.5:p.Asp254=
ENST00000375128.4:c.762T=	ENSP00000364270.4:p.Asp254=
ENST00000462523.5:c.*198T=	ENSP00000433006.1:n.*198T=
ENST00000485042.1:n.274T=
NM_000380.3:c.762T= , LRG_471t1:c.762T=	NP_000371.1:p.Asp254=
NR_027302.1:n.1110T=
XM_006717278.1:c.762T=	XP_006717341.1:p.Asp254=
XM_011518988.1:c.762T=	XP_011517290.1:p.Asp254=
XR_929839.1:n.1293T=
NM_001354975.1:c.636T=	NP_001341904.1:p.Asp212=
NR_149091.1:n.607T=
NR_149092.1:n.773T=
NR_149093.1:n.1299T=
NR_149094.1:n.1193T=
NM_000380.4:c.762T= MANE Select	NP_000371.1:p.Asp254=
NM_001354975.2:c.636T=	NP_001341904.1:p.Asp212=
NR_027302.2:n.1041T=
NR_149091.2:n.538T=
NR_149092.2:n.704T=
NR_149093.2:n.1230T=
NR_149094.2:n.1124T=