Canonical Allele Identifier: CA16592661
Gene: HUNK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31923801A>G , CM000683.2:g.31923801A>G GRCh38
NC_000021.8:g.33296113A>G , CM000683.1:g.33296113A>G GRCh37
NC_000021.7:g.32217984A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270112.7:c.262-667A>G MANE Select ENSP00000270112.2:n.262-667A>G
ENST00000270112.6:c.262-667A>G ENSP00000270112.2:n.262-667A>G
NM_014586.1:c.262-667A>G NP_055401.1:n.262-667A>G
XM_011529537.1:c.262-667A>G XP_011527839.1:n.262-667A>G
XM_011529537.2:c.262-667A>G XP_011527839.1:n.262-667A>G
NM_014586.2:c.262-667A>G MANE Select NP_055401.1:n.262-667A>G