Canonical Allele Identifier: CA10508047

Gene: XIAP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123886431C>G , CM000685.2:g.123886431C>G	GRCh38
NC_000023.10:g.123020281C>G , CM000685.1:g.123020281C>G	GRCh37
NC_000023.9:g.122847962C>G	NCBI36
NG_007264.1:g.31234C>G , LRG_19:g.31234C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422098.6:c.769C>G	ENSP00000405529.2:p.Pro257Ala
ENST00000371199.8:c.769C>G MANE Select	ENSP00000360242.3:p.Pro257Ala
ENST00000355640.3:c.769C>G	ENSP00000347858.3:p.Pro257Ala
ENST00000371199.7:c.769C>G	ENSP00000360242.3:p.Pro257Ala
ENST00000434753.7:c.769C>G	ENSP00000395230.3:p.Pro257Ala
ENST00000468503.1:n.93-2188C>G
ENST00000468691.5:n.157-2188C>G
ENST00000481776.5:n.143-2188C>G
ENST00000497640.1:n.100-2188C>G
ENST00000497906.5:n.207-2188C>G
NM_001167.3:c.769C>G , LRG_19t1:c.769C>G	NP_001158.2:p.Pro257Ala
NM_001204401.1:c.769C>G	NP_001191330.1:p.Pro257Ala
NR_037916.1:n.128-2188C>G
XM_006724754.2:c.769C>G	XP_006724817.1:p.Pro257Ala
XM_011531329.1:c.769C>G	XP_011529631.1:p.Pro257Ala
XM_011531329.2:c.769C>G	XP_011529631.1:p.Pro257Ala
NM_001167.4:c.769C>G MANE Select	NP_001158.2:p.Pro257Ala
NM_001204401.2:c.769C>G	NP_001191330.1:p.Pro257Ala
NM_001378590.1:c.769C>G	NP_001365519.1:p.Pro257Ala
NM_001378591.1:c.769C>G	NP_001365520.1:p.Pro257Ala
NM_001378592.1:c.769C>G	NP_001365521.1:p.Pro257Ala
NR_037916.2:n.242-2188C>G
NR_165803.1:n.224-2188C>G