Canonical Allele Identifier: CA486970496

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67776008C>T , CM000676.2:g.67776008C>T	GRCh38
NC_000014.8:g.68242725C>T , CM000676.1:g.68242725C>T	GRCh37
NC_000014.7:g.67312478C>T	NCBI36
NG_011836.1:g.45582G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.5073G>A MANE Select	NP_056161.2:p.Val1691=
ENST00000347230.9:c.5073G>A MANE Select	ENSP00000251119.5:p.Val1691=
NM_015346.3:c.5073G>A	NP_056161.2:p.Val1691=
ENST00000347230.8:c.5073G>A	ENSP00000251119.5:p.Val1691=
ENST00000554523.5:n.5210G>A
ENST00000554557.5:c.*3051G>A	ENSP00000450431.1:n.*3051G>A
ENST00000555452.1:c.5073G>A	ENSP00000450603.1:p.Val1691=
ENST00000676512.1:c.5073G>A	ENSP00000504552.1:p.Val1691=
ENST00000676620.1:c.4995G>A	ENSP00000504587.1:p.Val1665=
ENST00000678386.1:c.5118G>A	ENSP00000503677.1:p.Val1706=
XM_006720093.2:c.5073G>A	XP_006720156.1:p.Val1691=
XM_011536606.1:c.3564G>A	XP_011534908.1:p.Val1188=
XM_011536607.1:c.2748G>A	XP_011534909.1:p.Val916=
XM_011536608.1:c.2655G>A	XP_011534910.1:p.Val885=
XM_011536609.2:c.*89G>A	XP_011534911.1:n.*89G>A
XM_017021124.1:c.5073G>A	XP_016876613.1:p.Val1691=
XM_017021125.1:c.5073G>A	XP_016876614.1:p.Val1691=
XM_017021126.1:c.3564G>A	XP_016876615.1:p.Val1188=
XM_017021127.2:c.2748G>A	XP_016876616.1:p.Val916=
XM_017021128.1:c.2655G>A	XP_016876617.1:p.Val885=