Canonical Allele Identifier: CA357474655
Gene: ANTXR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072523C>G , CM000666.2:g.80072523C>G GRCh38
NC_000004.11:g.80993677C>G , CM000666.1:g.80993677C>G GRCh37
NC_000004.10:g.81212701C>G NCBI36
NG_015987.1:g.5801G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.38G>C MANE Select ENSP00000385575.2:p.Ser13Thr
ENST00000679571.1:c.-80+186G>C ENSP00000506307.1:n.-80+186G>C
ENST00000680913.1:c.38G>C ENSP00000505640.1:p.Ser13Thr
ENST00000681115.1:c.38G>C ENSP00000505618.1:p.Ser13Thr
ENST00000681710.1:c.-80+186G>C ENSP00000505865.1:n.-80+186G>C
ENST00000307333.7:c.38G>C ENSP00000306185.6:p.Ser13Thr
ENST00000346652.10:c.38G>C ENSP00000314883.6:p.Ser13Thr
ENST00000403729.6:c.38G>C ENSP00000385575.2:p.Ser13Thr
ENST00000404191.5:c.-79-869G>C ENSP00000384028.1:n.-79-869G>C
ENST00000506286.1:n.630-869G>C
ENST00000514959.1:n.248+6830G>C
NM_001145794.1:c.38G>C NP_001139266.1:p.Ser13Thr
NM_001286780.1:c.-79-869G>C NP_001273709.1:n.-79-869G>C
NM_001286781.1:c.-80+186G>C NP_001273710.1:n.-80+186G>C
NM_058172.5:c.38G>C NP_477520.2:p.Ser13Thr
XM_011531587.1:c.-79-869G>C XP_011529889.1:n.-79-869G>C
XM_011531587.3:c.-79-869G>C XP_011529889.1:n.-79-869G>C
NM_058172.6:c.38G>C MANE Select NP_477520.2:p.Ser13Thr
NM_001286780.2:c.-79-869G>C NP_001273709.1:n.-79-869G>C
NM_001286781.2:c.-80+186G>C NP_001273710.1:n.-80+186G>C
NM_001145794.2:c.38G>C NP_001139266.1:p.Ser13Thr