Canonical Allele Identifier: CA1064610682

Gene: ANTXR2

Linked Data

• dbSNP Id: rs1734857684
• gnomAD v3: 4-80072545-ACCGCTCCGCCACCATCCTGCGGCCGGGGG-A
• gnomAD v4: 4-80072545-ACCGCTCCGCCACCATCCTGCGGCCGGGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072548_80072576del , CM000666.2:g.80072548_80072576del	GRCh38
NC_000004.11:g.80993702_80993730del , CM000666.1:g.80993702_80993730del	GRCh37
NC_000004.10:g.81212726_81212754del	NCBI36
NG_015987.1:g.5750_5778del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-14_15del
ENST00000679571.1:c.-80+135_-80+163del	ENSP00000506307.1:n.-80+135_-80+163del
ENST00000680913.1:c.-14_15del
ENST00000681115.1:c.-14_15del
ENST00000681710.1:c.-80+135_-80+163del	ENSP00000505865.1:n.-80+135_-80+163del
ENST00000346652.10:c.-14_15del
ENST00000403729.6:c.-14_15del
ENST00000404191.5:c.-80+821_-80+849del	ENSP00000384028.1:n.-80+821_-80+849del
ENST00000506286.1:n.630-920_630-892del
ENST00000514959.1:n.248+6779_248+6807del
NM_001145794.1:c.-14_15del
NM_001286780.1:c.-80+821_-80+849del	NP_001273709.1:n.-80+821_-80+849del
NM_001286781.1:c.-80+135_-80+163del	NP_001273710.1:n.-80+135_-80+163del
NM_058172.5:c.-14_15del
XM_011531587.1:c.-80+821_-80+849del	XP_011529889.1:n.-80+821_-80+849del
XM_011531587.3:c.-80+821_-80+849del	XP_011529889.1:n.-80+821_-80+849del
NM_058172.6:c.-14_15del
NM_001286780.2:c.-80+821_-80+849del	NP_001273709.1:n.-80+821_-80+849del
NM_001286781.2:c.-80+135_-80+163del	NP_001273710.1:n.-80+135_-80+163del
NM_001145794.2:c.-14_15del