Canonical Allele Identifier: CA1866632270

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675508G= , CM000671.2:g.97675508G=	GRCh38
NC_000009.11:g.100437790G= , CM000671.1:g.100437790G=	GRCh37
NC_000009.10:g.99477611G=	NCBI36
NG_011642.1:g.26902C= , LRG_471:g.26902C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.753C= MANE Select	ENSP00000364270.5:p.Asn251=
ENST00000375128.4:c.753C=	ENSP00000364270.4:p.Asn251=
ENST00000462523.5:c.*189C=	ENSP00000433006.1:n.*189C=
ENST00000485042.1:n.265C=
NM_000380.3:c.753C= , LRG_471t1:c.753C=	NP_000371.1:p.Asn251=
NR_027302.1:n.1101C=
XM_006717278.1:c.753C=	XP_006717341.1:p.Asn251=
XM_011518988.1:c.753C=	XP_011517290.1:p.Asn251=
XR_929839.1:n.1284C=
NM_001354975.1:c.627C=	NP_001341904.1:p.Asn209=
NR_149091.1:n.598C=
NR_149092.1:n.764C=
NR_149093.1:n.1290C=
NR_149094.1:n.1184C=
NM_000380.4:c.753C= MANE Select	NP_000371.1:p.Asn251=
NM_001354975.2:c.627C=	NP_001341904.1:p.Asn209=
NR_027302.2:n.1032C=
NR_149091.2:n.529C=
NR_149092.2:n.695C=
NR_149093.2:n.1221C=
NR_149094.2:n.1115C=