Canonical Allele Identifier: CA2838381151

Gene: CNFN

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42389075C>T , CM000681.2:g.42389075C>T	GRCh38
NC_000019.9:g.42893227C>T , CM000681.1:g.42893227C>T	GRCh37
NC_000019.8:g.47585067C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222032.10:c.-2-36G>A MANE Select	ENSP00000222032.4:n.-2-36G>A
ENST00000222032.9:c.-2-36G>A	ENSP00000222032.4:n.-2-36G>A
ENST00000597255.1:c.-2-36G>A	ENSP00000469590.1:n.-2-36G>A
NM_032488.3:c.-2-36G>A	NP_115877.2:n.-2-36G>A
XM_005259332.2:c.38-36G>A	XP_005259389.1:n.38-36G>A
XM_011527396.1:c.38-36G>A	XP_011525698.1:n.38-36G>A
XM_011527397.1:c.38-36G>A	XP_011525699.1:n.38-36G>A
XM_005259332.3:c.38-36G>A	XP_005259389.1:n.38-36G>A
XM_011527396.2:c.38-36G>A	XP_011525698.1:n.38-36G>A
XM_011527397.2:c.38-36G>A	XP_011525699.1:n.38-36G>A
NM_032488.4:c.-2-36G>A MANE Select	NP_115877.2:n.-2-36G>A