Canonical Allele Identifier: CA1866632299

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675565G= , CM000671.2:g.97675565G=	GRCh38
NC_000009.11:g.100437847G= , CM000671.1:g.100437847G=	GRCh37
NC_000009.10:g.99477668G=	NCBI36
NG_011642.1:g.26845C= , LRG_471:g.26845C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.696C= MANE Select	ENSP00000364270.5:p.Ser232=
ENST00000375128.4:c.696C=	ENSP00000364270.4:p.Ser232=
ENST00000462523.5:c.*132C=	ENSP00000433006.1:n.*132C=
ENST00000485042.1:n.208C=
NM_000380.3:c.696C= , LRG_471t1:c.696C=	NP_000371.1:p.Ser232=
NR_027302.1:n.1044C=
XM_006717278.1:c.696C=	XP_006717341.1:p.Ser232=
XM_011518988.1:c.696C=	XP_011517290.1:p.Ser232=
XR_929839.1:n.1227C=
NM_001354975.1:c.570C=	NP_001341904.1:p.Ser190=
NR_149091.1:n.541C=
NR_149092.1:n.707C=
NR_149093.1:n.1233C=
NR_149094.1:n.1127C=
NM_000380.4:c.696C= MANE Select	NP_000371.1:p.Ser232=
NM_001354975.2:c.570C=	NP_001341904.1:p.Ser190=
NR_027302.2:n.975C=
NR_149091.2:n.472C=
NR_149092.2:n.638C=
NR_149093.2:n.1164C=
NR_149094.2:n.1058C=