Canonical Allele Identifier: CA14863925
Gene: PKNOX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43016067G>A , CM000683.2:g.43016067G>A GRCh38
NC_000021.8:g.44436177G>A , CM000683.1:g.44436177G>A GRCh37
NC_000021.7:g.43309246G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291547.10:c.523-841G>A MANE Select ENSP00000291547.4:n.523-841G>A
ENST00000291547.9:c.523-841G>A ENSP00000291547.4:n.523-841G>A
ENST00000432907.6:c.172-841G>A ENSP00000402243.2:n.172-841G>A
ENST00000480179.1:n.582-841G>A
ENST00000560448.5:c.*165-841G>A ENSP00000453486.1:n.*165-841G>A
NM_001286258.1:c.172-841G>A NP_001273187.1:n.172-841G>A
NM_004571.4:c.523-841G>A NP_004562.2:n.523-841G>A
XM_011529604.1:c.523-844G>A XP_011527906.1:n.523-844G>A
NM_001320694.1:c.523-844G>A NP_001307623.1:n.523-844G>A
NM_001320694.2:c.523-844G>A NP_001307623.1:n.523-844G>A
NM_004571.5:c.523-841G>A MANE Select NP_004562.2:n.523-841G>A
NM_001286258.2:c.172-841G>A NP_001273187.1:n.172-841G>A