Canonical Allele Identifier: CA390163382

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67761530G>A , CM000676.2:g.67761530G>A	GRCh38
NC_000014.8:g.68228247G>A , CM000676.1:g.68228247G>A	GRCh37
NC_000014.7:g.67298000G>A	NCBI36
NG_011836.1:g.60060C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.6424C>T MANE Select	NP_056161.2:p.Gln2142Ter
ENST00000347230.9:c.6424C>T MANE Select	ENSP00000251119.5:p.Gln2142Ter
NM_015346.3:c.6424C>T	NP_056161.2:p.Gln2142Ter
ENST00000347230.8:c.6424C>T	ENSP00000251119.5:p.Gln2142Ter
ENST00000394455.6:n.1687C>T
ENST00000554523.5:n.7179C>T
ENST00000554557.5:c.*4402C>T	ENSP00000450431.1:n.*4402C>T
ENST00000555452.1:c.6424C>T	ENSP00000450603.1:p.Gln2142Ter
ENST00000676512.1:c.6442C>T	ENSP00000504552.1:p.Gln2148Ter
ENST00000676620.1:c.6346C>T	ENSP00000504587.1:p.Gln2116Ter
ENST00000678386.1:c.6469C>T	ENSP00000503677.1:p.Gln2157Ter
XM_006720093.2:c.6424C>T	XP_006720156.1:p.Gln2142Ter
XM_011536606.1:c.4915C>T	XP_011534908.1:p.Gln1639Ter
XM_011536607.1:c.4099C>T	XP_011534909.1:p.Gln1367Ter
XM_011536608.1:c.4006C>T	XP_011534910.1:p.Gln1336Ter
XM_017021124.1:c.6442C>T	XP_016876613.1:p.Gln2148Ter
XM_017021125.1:c.6442C>T	XP_016876614.1:p.Gln2148Ter
XM_017021126.1:c.4933C>T	XP_016876615.1:p.Gln1645Ter
XM_017021127.2:c.4117C>T	XP_016876616.1:p.Gln1373Ter
XM_017021128.1:c.4024C>T	XP_016876617.1:p.Gln1342Ter