Canonical Allele Identifier: CA357474675
Gene: ANTXR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072533T>C , CM000666.2:g.80072533T>C GRCh38
NC_000004.11:g.80993687T>C , CM000666.1:g.80993687T>C GRCh37
NC_000004.10:g.81212711T>C NCBI36
NG_015987.1:g.5791A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.28A>G MANE Select ENSP00000385575.2:p.Ser10Gly
ENST00000679571.1:c.-80+176A>G ENSP00000506307.1:n.-80+176A>G
ENST00000680913.1:c.28A>G ENSP00000505640.1:p.Ser10Gly
ENST00000681115.1:c.28A>G ENSP00000505618.1:p.Ser10Gly
ENST00000681710.1:c.-80+176A>G ENSP00000505865.1:n.-80+176A>G
ENST00000307333.7:c.28A>G ENSP00000306185.6:p.Ser10Gly
ENST00000346652.10:c.28A>G ENSP00000314883.6:p.Ser10Gly
ENST00000403729.6:c.28A>G ENSP00000385575.2:p.Ser10Gly
ENST00000404191.5:c.-80+862A>G ENSP00000384028.1:n.-80+862A>G
ENST00000506286.1:n.630-879A>G
ENST00000514959.1:n.248+6820A>G
NM_001145794.1:c.28A>G NP_001139266.1:p.Ser10Gly
NM_001286780.1:c.-80+862A>G NP_001273709.1:n.-80+862A>G
NM_001286781.1:c.-80+176A>G NP_001273710.1:n.-80+176A>G
NM_058172.5:c.28A>G NP_477520.2:p.Ser10Gly
XM_011531587.1:c.-80+862A>G XP_011529889.1:n.-80+862A>G
XM_011531587.3:c.-80+862A>G XP_011529889.1:n.-80+862A>G
NM_058172.6:c.28A>G MANE Select NP_477520.2:p.Ser10Gly
NM_001286780.2:c.-80+862A>G NP_001273709.1:n.-80+862A>G
NM_001286781.2:c.-80+176A>G NP_001273710.1:n.-80+176A>G
NM_001145794.2:c.28A>G NP_001139266.1:p.Ser10Gly