Canonical Allele Identifier: CA440062326

Gene: ANTXR2

Linked Data

• dbSNP Id: rs1170768745
• gnomAD v2: 4-80905077-A-G
• gnomAD v4: 4-79983923-A-G
• MyVariant Identifiers: chr4:g.80905077A>G (hg19) ; chr4:g.79983923A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.79983923A>G , CM000666.2:g.79983923A>G	GRCh38
NC_000004.11:g.80905077A>G , CM000666.1:g.80905077A>G	GRCh37
NC_000004.10:g.81124101A>G	NCBI36
NG_015987.1:g.94401T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403729.7:c.1134T>C MANE Select	ENSP00000385575.2:p.Ala378=
ENST00000679571.1:c.903T>C	ENSP00000506307.1:p.Ala301=
ENST00000680913.1:c.1134T>C	ENSP00000505640.1:p.Ala378=
ENST00000681115.1:c.1134T>C	ENSP00000505618.1:p.Ala378=
ENST00000681710.1:c.903T>C	ENSP00000505865.1:p.Ala301=
ENST00000307333.7:c.1134T>C	ENSP00000306185.6:p.Ala378=
ENST00000346652.10:c.825T>C	ENSP00000314883.6:p.Ala275=
ENST00000403729.6:c.1134T>C	ENSP00000385575.2:p.Ala378=
ENST00000404191.5:c.903T>C	ENSP00000384028.1:p.Ala301=
ENST00000449651.5:c.*284T>C	ENSP00000413700.1:n.*284T>C
NM_001145794.1:c.1134T>C	NP_001139266.1:p.Ala378=
NM_001286780.1:c.903T>C	NP_001273709.1:p.Ala301=
NM_001286781.1:c.903T>C	NP_001273710.1:p.Ala301=
NM_058172.5:c.1134T>C	NP_477520.2:p.Ala378=
XM_011531587.1:c.903T>C	XP_011529889.1:p.Ala301=
XM_011531587.3:c.903T>C	XP_011529889.1:p.Ala301=
NM_058172.6:c.1134T>C MANE Select	NP_477520.2:p.Ala378=
NM_001286780.2:c.903T>C	NP_001273709.1:p.Ala301=
NM_001286781.2:c.903T>C	NP_001273710.1:p.Ala301=
NM_001145794.2:c.1134T>C	NP_001139266.1:p.Ala378=