Canonical Allele Identifier: CA2578126655

Gene: ANTXR2

Linked Data

• gnomAD v4: 4-80072658-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072664del , CM000666.2:g.80072664del	GRCh38
NC_000004.11:g.80993818del , CM000666.1:g.80993818del	GRCh37
NC_000004.10:g.81212842del	NCBI36
NG_015987.1:g.5665del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-99del MANE Select	ENSP00000385575.2:n.-99del
ENST00000679571.1:c.-80+50del	ENSP00000506307.1:n.-80+50del
ENST00000680913.1:c.-99del	ENSP00000505640.1:n.-99del
ENST00000681115.1:c.-99del	ENSP00000505618.1:n.-99del
ENST00000681710.1:c.-80+50del	ENSP00000505865.1:n.-80+50del
ENST00000346652.10:c.-99del	ENSP00000314883.6:n.-99del
ENST00000403729.6:c.-99del	ENSP00000385575.2:n.-99del
ENST00000404191.5:c.-80+736del	ENSP00000384028.1:n.-80+736del
ENST00000506286.1:n.630-1005del
ENST00000514959.1:n.248+6694del
NM_001145794.1:c.-99del	NP_001139266.1:n.-99del
NM_001286780.1:c.-80+736del	NP_001273709.1:n.-80+736del
NM_001286781.1:c.-80+50del	NP_001273710.1:n.-80+50del
NM_058172.5:c.-99del	NP_477520.2:n.-99del
XM_011531587.1:c.-80+736del	XP_011529889.1:n.-80+736del
XM_011531587.3:c.-80+736del	XP_011529889.1:n.-80+736del
NM_058172.6:c.-99del MANE Select	NP_477520.2:n.-99del
NM_001286780.2:c.-80+736del	NP_001273709.1:n.-80+736del
NM_001286781.2:c.-80+50del	NP_001273710.1:n.-80+50del
NM_001145794.2:c.-99del	NP_001139266.1:n.-99del