Canonical Allele Identifier: CA440062327

Gene: ANTXR2

Linked Data

• MyVariant Identifiers: chr4:g.80905077A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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