Canonical Allele Identifier: CA10336819

Gene: XG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2794595C>T , CM000685.2:g.2794595C>T	GRCh38
NC_000023.10:g.2712636C>T , CM000685.1:g.2712636C>T	GRCh37
NC_000023.9:g.2722636C>T	NCBI36
NG_011627.1:g.47544C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381174.10:c.314C>T	ENSP00000370566.5:p.Pro105Leu
ENST00000419513.7:c.248C>T	ENSP00000411004.3:p.Pro83Leu
ENST00000509484.3:c.248C>T	ENSP00000430005.2:p.Pro83Leu
ENST00000644266.2:c.314C>T MANE Select	ENSP00000494087.1:p.Pro105Leu
ENST00000381174.9:c.314C>T	ENSP00000370566.5:p.Pro105Leu
ENST00000419513.6:c.314C>T	ENSP00000411004.2:p.Pro105Leu
ENST00000509484.2:c.248C>T	ENSP00000430005.1:p.Pro83Leu
ENST00000519244.1:n.61C>T
NM_001141919.1:c.314C>T	NP_001135391.1:p.Pro105Leu
NM_001141920.1:c.317C>T	NP_001135392.1:p.Pro106Leu
NM_175569.2:c.314C>T	NP_780778.1:p.Pro105Leu
XM_005274587.2:c.317C>T	XP_005274644.1:p.Pro106Leu
XM_006724512.2:c.317C>T	XP_006724575.1:p.Pro106Leu
XM_011545572.1:c.317C>T	XP_011543874.1:p.Pro106Leu
XM_011545573.1:c.317C>T	XP_011543875.1:p.Pro106Leu
XM_011545574.1:c.229C>T	XP_011543876.1:p.Arg77Cys
XM_011545575.1:c.317C>T	XP_011543877.1:p.Pro106Leu
XM_011545576.1:c.229C>T	XP_011543878.1:p.Arg77Cys
XM_005274587.4:c.317C>T	XP_005274644.1:p.Pro106Leu
XM_011545575.3:c.317C>T	XP_011543877.1:p.Pro106Leu
XM_017029787.2:c.275C>T	XP_016885276.1:p.Pro92Leu
NM_001141919.2:c.314C>T MANE Select	NP_001135391.1:p.Pro105Leu
NM_001141920.2:c.317C>T	NP_001135392.1:p.Pro106Leu
NM_175569.3:c.314C>T	NP_780778.1:p.Pro105Leu