Canonical Allele Identifier: CA1866632264

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675500T= , CM000671.2:g.97675500T=	GRCh38
NC_000009.11:g.100437782T= , CM000671.1:g.100437782T=	GRCh37
NC_000009.10:g.99477603T=	NCBI36
NG_011642.1:g.26910A= , LRG_471:g.26910A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.761A= MANE Select	ENSP00000364270.5:p.Asp254=
ENST00000375128.4:c.761A=	ENSP00000364270.4:p.Asp254=
ENST00000462523.5:c.*197A=	ENSP00000433006.1:n.*197A=
ENST00000485042.1:n.273A=
NM_000380.3:c.761A= , LRG_471t1:c.761A=	NP_000371.1:p.Asp254=
NR_027302.1:n.1109A=
XM_006717278.1:c.761A=	XP_006717341.1:p.Asp254=
XM_011518988.1:c.761A=	XP_011517290.1:p.Asp254=
XR_929839.1:n.1292A=
NM_001354975.1:c.635A=	NP_001341904.1:p.Asp212=
NR_149091.1:n.606A=
NR_149092.1:n.772A=
NR_149093.1:n.1298A=
NR_149094.1:n.1192A=
NM_000380.4:c.761A= MANE Select	NP_000371.1:p.Asp254=
NM_001354975.2:c.635A=	NP_001341904.1:p.Asp212=
NR_027302.2:n.1040A=
NR_149091.2:n.537A=
NR_149092.2:n.703A=
NR_149093.2:n.1229A=
NR_149094.2:n.1123A=