Canonical Allele Identifier: CA748681885

Gene: HUNK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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