Canonical Allele Identifier: CA1866632294

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675553T= , CM000671.2:g.97675553T=	GRCh38
NC_000009.11:g.100437835T= , CM000671.1:g.100437835T=	GRCh37
NC_000009.10:g.99477656T=	NCBI36
NG_011642.1:g.26857A= , LRG_471:g.26857A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.708A= MANE Select	ENSP00000364270.5:p.Lys236=
ENST00000375128.4:c.708A=	ENSP00000364270.4:p.Lys236=
ENST00000462523.5:c.*144A=	ENSP00000433006.1:n.*144A=
ENST00000485042.1:n.220A=
NM_000380.3:c.708A= , LRG_471t1:c.708A=	NP_000371.1:p.Lys236=
NR_027302.1:n.1056A=
XM_006717278.1:c.708A=	XP_006717341.1:p.Lys236=
XM_011518988.1:c.708A=	XP_011517290.1:p.Lys236=
XR_929839.1:n.1239A=
NM_001354975.1:c.582A=	NP_001341904.1:p.Lys194=
NR_149091.1:n.553A=
NR_149092.1:n.719A=
NR_149093.1:n.1245A=
NR_149094.1:n.1139A=
NM_000380.4:c.708A= MANE Select	NP_000371.1:p.Lys236=
NM_001354975.2:c.582A=	NP_001341904.1:p.Lys194=
NR_027302.2:n.987A=
NR_149091.2:n.484A=
NR_149092.2:n.650A=
NR_149093.2:n.1176A=
NR_149094.2:n.1070A=