Canonical Allele Identifier: CA7240605
Community Standard Title: NM_015346.4(ZFYVE26):c.1161C>G (p.Leu387=)
Gene: ZFYVE26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67805475G>C , CM000676.2:g.67805475G>C GRCh38
NC_000014.8:g.68272192G>C , CM000676.1:g.68272192G>C GRCh37
NC_000014.7:g.67341945G>C NCBI36
NG_011836.1:g.16115C>G

Transcript Alleles

HGVS Amino-acid Change
NM_015346.4:c.1161C>G MANE Select NP_056161.2:p.Leu387=
ENST00000347230.9:c.1161C>G MANE Select ENSP00000251119.5:p.Leu387=
NM_015346.3:c.1161C>G NP_056161.2:p.Leu387=
ENST00000347230.8:c.1161C>G ENSP00000251119.5:p.Leu387=
ENST00000554523.5:n.1298C>G
ENST00000554557.5:c.1161C>G ENSP00000450431.1:p.Leu387=
ENST00000555452.1:c.1161C>G ENSP00000450603.1:p.Leu387=
ENST00000557366.5:n.1296C>G
ENST00000557407.1:n.1296C>G
ENST00000676512.1:c.1161C>G ENSP00000504552.1:p.Leu387=
ENST00000676620.1:c.1161C>G ENSP00000504587.1:p.Leu387=
ENST00000677026.1:c.1161C>G ENSP00000503710.1:p.Leu387=
ENST00000678382.1:c.*156C>G ENSP00000504130.1:n.*156C>G
ENST00000678386.1:c.1161C>G ENSP00000503677.1:p.Leu387=
XM_006720093.2:c.1161C>G XP_006720156.1:p.Leu387=
XM_011536606.1:c.-260C>G XP_011534908.1:n.-260C>G
XM_011536609.1:c.1161C>G XP_011534911.1:p.Leu387=
XM_011536609.2:c.1161C>G XP_011534911.1:p.Leu387=
XM_017021124.1:c.1161C>G XP_016876613.1:p.Leu387=
XM_017021125.1:c.1161C>G XP_016876614.1:p.Leu387=
XM_017021126.1:c.-260C>G XP_016876615.1:n.-260C>G