Canonical Allele Identifier: CA3151946629
Community Standard Title: NM_001018111.3(PODXL):c.1101+122C=
Gene: PODXL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.131508829G= , CM000669.2:g.131508829G= GRCh38
NC_000007.13:g.131193588G= , CM000669.1:g.131193588G= GRCh37
NC_000007.12:g.130844128G= NCBI36
NG_042104.1:g.52789C=

Transcript Alleles

HGVS Amino-acid Change
NM_001018111.3:c.1101+122C= MANE Select NP_001018121.1:n.1101+122C=
ENST00000378555.8:c.1101+122C= MANE Select ENSP00000367817.3:n.1101+122C=
NM_001018111.2:c.1101+122C= NP_001018121.1:n.1101+122C=
NM_005397.3:c.1005+122C= NP_005388.2:n.1005+122C=
NM_005397.4:c.1005+122C= NP_005388.2:n.1005+122C=
ENST00000322985.9:c.1005+122C= ENSP00000319782.9:n.1005+122C=
ENST00000378555.7:c.1101+122C= ENSP00000367817.3:n.1101+122C=
ENST00000446198.5:c.*366+122C= ENSP00000390152.1:n.*366+122C=
ENST00000487965.1:n.452+122C=