Canonical Allele Identifier: CA357472566

Gene: ANTXR2

Linked Data

• MyVariant Identifiers: chr4:g.80975496A>C (hg19) ; chr4:g.80054342A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80054342A>C , CM000666.2:g.80054342A>C	GRCh38
NC_000004.11:g.80975496A>C , CM000666.1:g.80975496A>C	GRCh37
NC_000004.10:g.81194520A>C	NCBI36
NG_015987.1:g.23982T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.566T>G MANE Select	ENSP00000385575.2:p.Ile189Ser
ENST00000679571.1:c.335T>G	ENSP00000506307.1:p.Ile112Ser
ENST00000680913.1:c.566T>G	ENSP00000505640.1:p.Ile189Ser
ENST00000681115.1:c.566T>G	ENSP00000505618.1:p.Ile189Ser
ENST00000681710.1:c.335T>G	ENSP00000505865.1:p.Ile112Ser
ENST00000307333.7:c.566T>G	ENSP00000306185.6:p.Ile189Ser
ENST00000346652.10:c.566T>G	ENSP00000314883.6:p.Ile189Ser
ENST00000403729.6:c.566T>G	ENSP00000385575.2:p.Ile189Ser
ENST00000404191.5:c.335T>G	ENSP00000384028.1:p.Ile112Ser
ENST00000449651.5:c.335T>G	ENSP00000413700.1:p.Ile112Ser
ENST00000514959.1:n.518T>G
NM_001145794.1:c.566T>G	NP_001139266.1:p.Ile189Ser
NM_001286780.1:c.335T>G	NP_001273709.1:p.Ile112Ser
NM_001286781.1:c.335T>G	NP_001273710.1:p.Ile112Ser
NM_058172.5:c.566T>G	NP_477520.2:p.Ile189Ser
XM_011531587.1:c.335T>G	XP_011529889.1:p.Ile112Ser
XM_011531587.3:c.335T>G	XP_011529889.1:p.Ile112Ser
NM_058172.6:c.566T>G MANE Select	NP_477520.2:p.Ile189Ser
NM_001286780.2:c.335T>G	NP_001273709.1:p.Ile112Ser
NM_001286781.2:c.335T>G	NP_001273710.1:p.Ile112Ser
NM_001145794.2:c.566T>G	NP_001139266.1:p.Ile189Ser