Canonical Allele Identifier: CA1866632260

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675493C= , CM000671.2:g.97675493C=	GRCh38
NC_000009.11:g.100437775C= , CM000671.1:g.100437775C=	GRCh37
NC_000009.10:g.99477596C=	NCBI36
NG_011642.1:g.26917G= , LRG_471:g.26917G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.768G= MANE Select	ENSP00000364270.5:p.Met256=
ENST00000375128.4:c.768G=	ENSP00000364270.4:p.Met256=
ENST00000462523.5:c.*204G=	ENSP00000433006.1:n.*204G=
ENST00000485042.1:n.280G=
NM_000380.3:c.768G= , LRG_471t1:c.768G=	NP_000371.1:p.Met256=
NR_027302.1:n.1116G=
XM_006717278.1:c.768G=	XP_006717341.1:p.Met256=
XM_011518988.1:c.768G=	XP_011517290.1:p.Met256=
NM_001354975.1:c.642G=	NP_001341904.1:p.Met214=
NR_149091.1:n.613G=
NR_149092.1:n.779G=
NR_149093.1:n.1305G=
NR_149094.1:n.1199G=
NM_000380.4:c.768G= MANE Select	NP_000371.1:p.Met256=
NM_001354975.2:c.642G=	NP_001341904.1:p.Met214=
NR_027302.2:n.1047G=
NR_149091.2:n.544G=
NR_149092.2:n.710G=
NR_149093.2:n.1236G=
NR_149094.2:n.1130G=