Canonical Allele Identifier: CA374185489

Gene: XPA

Linked Data

• MyVariant Identifiers: chr9:g.100437832C>G (hg19) ; chr9:g.97675550C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675550C>G , CM000671.2:g.97675550C>G	GRCh38
NC_000009.11:g.100437832C>G , CM000671.1:g.100437832C>G	GRCh37
NC_000009.10:g.99477653C>G	NCBI36
NG_011642.1:g.26860G>C , LRG_471:g.26860G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.711G>C MANE Select	ENSP00000364270.5:p.Arg237Ser
ENST00000375128.4:c.711G>C	ENSP00000364270.4:p.Arg237Ser
ENST00000462523.5:c.*147G>C	ENSP00000433006.1:n.*147G>C
ENST00000485042.1:n.223G>C
NM_000380.3:c.711G>C , LRG_471t1:c.711G>C	NP_000371.1:p.Arg237Ser
NR_027302.1:n.1059G>C
XM_006717278.1:c.711G>C	XP_006717341.1:p.Arg237Ser
XM_011518988.1:c.711G>C	XP_011517290.1:p.Arg237Ser
XR_929839.1:n.1242G>C
NM_001354975.1:c.585G>C	NP_001341904.1:p.Arg195Ser
NR_149091.1:n.556G>C
NR_149092.1:n.722G>C
NR_149093.1:n.1248G>C
NR_149094.1:n.1142G>C
NM_000380.4:c.711G>C MANE Select	NP_000371.1:p.Arg237Ser
NM_001354975.2:c.585G>C	NP_001341904.1:p.Arg195Ser
NR_027302.2:n.990G>C
NR_149091.2:n.487G>C
NR_149092.2:n.653G>C
NR_149093.2:n.1179G>C
NR_149094.2:n.1073G>C