Canonical Allele Identifier: CA100504993

Gene: ANTXR2

Linked Data

• dbSNP Id: rs970556159
• gnomAD v3: 4-80072750-AG-A
• gnomAD v4: 4-80072750-AG-A
• MyVariant Identifiers: chr4:g.80993905del (hg19) ; chr4:g.80072751del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072753del , CM000666.2:g.80072753del	GRCh38
NC_000004.11:g.80993907del , CM000666.1:g.80993907del	GRCh37
NC_000004.10:g.81212931del	NCBI36
NG_015987.1:g.5573del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-191del MANE Select	ENSP00000385575.2:n.-191del
ENST00000679571.1:c.-122del	ENSP00000506307.1:n.-122del
ENST00000681115.1:c.-191del	ENSP00000505618.1:n.-191del
ENST00000681710.1:c.-122del	ENSP00000505865.1:n.-122del
ENST00000403729.6:c.-191del	ENSP00000385575.2:n.-191del
ENST00000404191.5:c.-80+644del	ENSP00000384028.1:n.-80+644del
ENST00000506286.1:n.630-1097del
ENST00000514959.1:n.248+6602del
NM_001145794.1:c.-191del	NP_001139266.1:n.-191del
NM_001286780.1:c.-80+644del	NP_001273709.1:n.-80+644del
NM_001286781.1:c.-122del	NP_001273710.1:n.-122del
NM_058172.5:c.-191del	NP_477520.2:n.-191del
XM_011531587.1:c.-80+644del	XP_011529889.1:n.-80+644del
XM_011531587.3:c.-80+644del	XP_011529889.1:n.-80+644del
NM_058172.6:c.-191del MANE Select	NP_477520.2:n.-191del
NM_001286780.2:c.-80+644del	NP_001273709.1:n.-80+644del
NM_001286781.2:c.-122del	NP_001273710.1:n.-122del
NM_001145794.2:c.-191del	NP_001139266.1:n.-191del