Canonical Allele Identifier: CA1692734
Gene: ANTXR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.69013519G>A , CM000664.2:g.69013519G>A GRCh38
NC_000002.11:g.69240651G>A , CM000664.1:g.69240651G>A GRCh37
NC_000002.10:g.69094155G>A NCBI36
NG_012649.1:g.5376G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303714.9:c.20G>A MANE Select ENSP00000301945.4:p.Arg7Lys
ENST00000463335.2:c.20G>A ENSP00000506719.1:p.Arg7Lys
ENST00000481119.2:n.344G>A
ENST00000482235.2:c.20G>A ENSP00000430776.2:p.Arg7Lys
ENST00000681568.1:n.163G>A
ENST00000681816.1:c.20G>A ENSP00000505171.1:p.Arg7Lys
ENST00000303714.8:c.20G>A ENSP00000301945.4:p.Arg7Lys
ENST00000409349.7:c.20G>A ENSP00000386494.3:p.Arg7Lys
ENST00000409829.7:c.20G>A ENSP00000387058.3:p.Arg7Lys
ENST00000463335.1:n.163G>A
NM_018153.3:c.20G>A NP_060623.2:p.Arg7Lys
NM_032208.2:c.20G>A NP_115584.1:p.Arg7Lys
NM_053034.2:c.20G>A NP_444262.1:p.Arg7Lys
XM_011533124.1:c.20G>A XP_011531426.1:p.Arg7Lys
XR_939725.1:n.167G>A
XR_939726.1:n.167G>A
XM_017005075.2:c.20G>A XP_016860564.1:p.Arg7Lys
XM_017005076.2:c.20G>A XP_016860565.1:p.Arg7Lys
XM_017005077.2:c.20G>A XP_016860566.1:p.Arg7Lys
NM_032208.3:c.20G>A MANE Select NP_115584.1:p.Arg7Lys