Canonical Allele Identifier: CA390168577

Gene: ZFYVE26

Linked Data

• MyVariant Identifiers: chr14:g.68242820G>T (hg19) ; chr14:g.67776103G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67776103G>T , CM000676.2:g.67776103G>T	GRCh38
NC_000014.8:g.68242820G>T , CM000676.1:g.68242820G>T	GRCh37
NC_000014.7:g.67312573G>T	NCBI36
NG_011836.1:g.45487C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4978C>A MANE Select	ENSP00000251119.5:p.Leu1660Met
ENST00000676512.1:c.4978C>A	ENSP00000504552.1:p.Leu1660Met
ENST00000676620.1:c.4975-75C>A	ENSP00000504587.1:n.4975-75C>A
ENST00000678386.1:c.5023C>A	ENSP00000503677.1:p.Leu1675Met
ENST00000347230.8:c.4978C>A	ENSP00000251119.5:p.Leu1660Met
ENST00000554523.5:n.5115C>A
ENST00000554557.5:c.*2956C>A	ENSP00000450431.1:n.*2956C>A
ENST00000555452.1:c.4978C>A	ENSP00000450603.1:p.Leu1660Met
NM_015346.3:c.4978C>A	NP_056161.2:p.Leu1660Met
XM_006720093.2:c.4978C>A	XP_006720156.1:p.Leu1660Met
XM_011536606.1:c.3469C>A	XP_011534908.1:p.Leu1157Met
XM_011536607.1:c.2653C>A	XP_011534909.1:p.Leu885Met
XM_011536608.1:c.2560C>A	XP_011534910.1:p.Leu854Met
XM_011536609.1:c.4995C>A	XP_011534911.1:p.Phe1665Leu
XM_011536609.2:c.4995C>A	XP_011534911.1:p.Phe1665Leu
XM_017021124.1:c.4978C>A	XP_016876613.1:p.Leu1660Met
XM_017021125.1:c.4978C>A	XP_016876614.1:p.Leu1660Met
XM_017021126.1:c.3469C>A	XP_016876615.1:p.Leu1157Met
XM_017021127.2:c.2653C>A	XP_016876616.1:p.Leu885Met
XM_017021128.1:c.2560C>A	XP_016876617.1:p.Leu854Met
NM_015346.4:c.4978C>A MANE Select	NP_056161.2:p.Leu1660Met