Canonical Allele Identifier: CA2531045819

Gene: ANTXR2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072135_80072136insGCGGGCCACGCTCCCA , CM000666.2:g.80072135_80072136insGCGGGCCACGCTCCCA	GRCh38
NC_000004.11:g.80993289_80993290insGCGGGCCACGCTCCCA , CM000666.1:g.80993289_80993290insGCGGGCCACGCTCCCA	GRCh37
NC_000004.10:g.81212313_81212314insGCGGGCCACGCTCCCA	NCBI36
NG_015987.1:g.6194_6195insCGTGGCCCGCTGGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.152+279_152+280insCGTGGCCCGCTGGGAG MANE Select	ENSP00000385575.2:n.152+279_152+280insCGTGGCCCGCTGGGAG
ENST00000679571.1:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	ENSP00000506307.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
ENST00000680913.1:c.152+279_152+280insCGTGGCCCGCTGGGAG	ENSP00000505640.1:n.152+279_152+280insCGTGGCCCGCTGGGAG
ENST00000681115.1:c.152+279_152+280insCGTGGCCCGCTGGGAG	ENSP00000505618.1:n.152+279_152+280insCGTGGCCCGCTGGGAG
ENST00000681710.1:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	ENSP00000505865.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
ENST00000307333.7:c.152+279_152+280insCGTGGCCCGCTGGGAG	ENSP00000306185.6:n.152+279_152+280insCGTGGCCCGCTGGGAG
ENST00000346652.10:c.152+279_152+280insCGTGGCCCGCTGGGAG	ENSP00000314883.6:n.152+279_152+280insCGTGGCCCGCTGGGAG
ENST00000403729.6:c.152+279_152+280insCGTGGCCCGCTGGGAG	ENSP00000385575.2:n.152+279_152+280insCGTGGCCCGCTGGGAG
ENST00000404191.5:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	ENSP00000384028.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
ENST00000506286.1:n.630-476_630-475insCGTGGCCCGCTGGGAG
ENST00000514959.1:n.248+7223_248+7224insCGTGGCCCGCTGGGAG
NM_001145794.1:c.152+279_152+280insCGTGGCCCGCTGGGAG	NP_001139266.1:n.152+279_152+280insCGTGGCCCGCTGGGAG
NM_001286780.1:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	NP_001273709.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
NM_001286781.1:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	NP_001273710.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
NM_058172.5:c.152+279_152+280insCGTGGCCCGCTGGGAG	NP_477520.2:n.152+279_152+280insCGTGGCCCGCTGGGAG
XM_011531587.1:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	XP_011529889.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
XM_011531587.3:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	XP_011529889.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
NM_058172.6:c.152+279_152+280insCGTGGCCCGCTGGGAG MANE Select	NP_477520.2:n.152+279_152+280insCGTGGCCCGCTGGGAG
NM_001286780.2:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	NP_001273709.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
NM_001286781.2:c.-79-476_-79-475insCGTGGCCCGCTGGGAG	NP_001273710.1:n.-79-476_-79-475insCGTGGCCCGCTGGGAG
NM_001145794.2:c.152+279_152+280insCGTGGCCCGCTGGGAG	NP_001139266.1:n.152+279_152+280insCGTGGCCCGCTGGGAG